Year |
Citation |
Score |
2023 |
Lu B, Ohayon YP, Woloszyn K, Yang CF, Yoder JB, Rothschild LJ, Wind SJ, Hendrickson WA, Mao C, Seeman NC, Canary JW, Sha R, Vecchioni S. Heterobimetallic Base Pair Programming in Designer 3D DNA Crystals. Journal of the American Chemical Society. PMID 37530628 DOI: 10.1021/jacs.3c05478 |
0.75 |
|
2023 |
Vecchioni S, Lu B, Livernois W, Ohayon YP, Yoder JB, Yang CF, Woloszyn K, Bernfeld W, Anantram MP, Canary JW, Hendrickson WA, Rothschild LJ, Mao C, Wind SJ, Seeman NC, et al. Metal-Mediated DNA Nanotechnology in 3D: Structural Library by Templated Diffraction. Advanced Materials (Deerfield Beach, Fla.). e2210938. PMID 37268326 DOI: 10.1002/adma.202210938 |
0.756 |
|
2023 |
Vecchioni S, Lu B, Livernois W, Ohayon YP, Yoder JB, Yang CF, Woloszyn K, Bernfeld W, Anantram MP, Canary JW, Hendrickson WA, Rothschild LJ, Mao C, Wind SJ, Seeman NC, et al. Metal-Mediated DNA Nanotechnology in 3D: Structural Library by Templated Diffraction. Advanced Materials (Deerfield Beach, Fla.). e2201938. PMID 36939292 DOI: 10.1002/adma.202201938 |
0.755 |
|
2022 |
Lu B, Vecchioni S, Ohayon YP, Woloszyn K, Markus T, Mao C, Seeman NC, Canary JW, Sha R. Highly Symmetric, Self-Assembling 3D DNA Crystals with Cubic and Trigonal Lattices. Small (Weinheim An Der Bergstrasse, Germany). e2205830. PMID 36408817 DOI: 10.1002/smll.202205830 |
0.735 |
|
2022 |
Lu B, Vecchioni S, Ohayon YP, Canary JW, Sha R. The Wending Rhombus: Self-Assembling 3D DNA Crystals. Biophysical Journal. PMID 36004779 DOI: 10.1016/j.bpj.2022.08.019 |
0.69 |
|
2022 |
Wang X, Sha R, Knowlton WB, Seeman NC, Canary JW, Yurke B. Exciton Delocalization in a DNA-Templated Organic Semiconductor Dimer Assembly. Acs Nano. PMID 34979076 DOI: 10.1021/acsnano.1c09143 |
0.521 |
|
2021 |
Wang X, Deshmukh R, Sha R, Birktoft JJ, Menon V, Seeman NC, Canary JW. Orienting an Organic Semiconductor into DNA 3D Arrays by Covalent Bonds. Angewandte Chemie (International Ed. in English). PMID 34847266 DOI: 10.1002/anie.202115155 |
0.486 |
|
2019 |
Pei H, Sha R, Wang X, Zheng M, Fan C, Canary JW, Seeman NC. Organizing End-Site-Specific SWCNTs in Specific Loci Using DNA. Journal of the American Chemical Society. PMID 31282152 DOI: 10.1021/Jacs.9B03432 |
0.439 |
|
2018 |
Wang X, Li C, Niu D, Sha R, Seeman NC, Canary JW. The Construction of a DNA Origami Based Molecular Electro-Optical Modulator. Nano Letters. PMID 29430930 DOI: 10.1021/Acs.Nanolett.8B00332 |
0.505 |
|
2017 |
Wang X, Sha R, Kristiansen M, Hernandez C, Hao Y, Mao C, Canary JW, Seeman NC. An Organic Semiconductor Organized into 3D DNA Arrays by "Bottom-up" Rational Design. Angewandte Chemie (International Ed. in English). PMID 28466984 DOI: 10.1002/Anie.201700462 |
0.518 |
|
2016 |
Mortezaei S, Catarineu NR, Canary JW. Dial-in selection of any of four stereochemical outcomes among two substrates by in situ stereo-reconfiguration of a single ambidextrous catalyst Tetrahedron Letters. 57: 459-462. DOI: 10.1016/J.Tetlet.2015.12.015 |
0.717 |
|
2015 |
Mortezaei S, Catarineu NR, Duan X, Hu C, Canary JW. Redox-configurable ambidextrous catalysis: structural and mechanistic insight. Chemical Science. 6: 5904-5912. PMID 29861915 DOI: 10.1039/C5Sc02144H |
0.754 |
|
2015 |
Niu D, Jiang H, Sha R, Canary JW, Seeman NC. The unusual and dynamic character of PX-DNA. Nucleic Acids Research. 43: 7201-6. PMID 26184876 DOI: 10.1093/Nar/Gkv739 |
0.461 |
|
2015 |
Mortezaei S, Catarineu NR, Duan X, Hu C, Canary JW. Redox-configurable ambidextrous catalysis: Structural and mechanistic insight Chemical Science. 6: 5904-5912. DOI: 10.1039/c5sc02144h |
0.733 |
|
2014 |
Li D, Wang X, Shi F, Sha R, Seeman NC, Canary JW. Templated DNA ligation with thiol chemistry. Organic & Biomolecular Chemistry. 12: 8823-7. PMID 25283556 DOI: 10.1039/C4Ob01552E |
0.59 |
|
2014 |
Udomprasert A, Bongiovanni MN, Sha R, Sherman WB, Wang T, Arora PS, Canary JW, Gras SL, Seeman NC. Amyloid fibrils nucleated and organized by DNA origami constructions. Nature Nanotechnology. 9: 537-41. PMID 24880222 DOI: 10.1038/Nnano.2014.102 |
0.45 |
|
2014 |
Isaacman S, Buckley M, Wang X, Wang EY, Liebes L, Canary JW. Targeted amplification of delivery to cell surface receptors by dendrimer self-assembly. Bioorganic & Medicinal Chemistry Letters. 24: 1290-3. PMID 24513050 DOI: 10.1016/J.Bmcl.2014.01.063 |
0.718 |
|
2013 |
Ye M, Guillaume J, Liu Y, Sha R, Wang R, Seeman NC, Canary JW. Site-specific inter-strand cross-links of DNA duplexes. Chemical Science (Royal Society of Chemistry : 2010). 4: 1319-1329. PMID 23894693 DOI: 10.1039/C2Sc21775A |
0.468 |
|
2013 |
Royzen M, Canary JW. Structural parameters of Zn(II) complexes of 8-hydroxyquinoline-based tripodal ligands affect fluorescence quantum yield Polyhedron. 58: 85-91. DOI: 10.1016/j.poly.2012.11.027 |
0.674 |
|
2012 |
Wang X, Canary JW. Rapid catalyst-free hydrazone ligation: protein-pyridoxal phosphoramides. Bioconjugate Chemistry. 23: 2329-34. PMID 23185966 DOI: 10.1021/Bc300430K |
0.419 |
|
2012 |
Liu Y, Wang R, Ding L, Sha R, Seeman NC, Canary JW. Templated synthesis of nylon nucleic acids and characterization by nuclease digestion. Chemical Science (Royal Society of Chemistry : 2010). 3: 1930-1937. PMID 23125913 DOI: 10.1039/C2Sc20129A |
0.477 |
|
2012 |
Wang X, Bergenfeld I, Arora PS, Canary JW. Reversible redox reconfiguration of secondary structures in a designed peptide. Angewandte Chemie (International Ed. in English). 51: 12099-101. PMID 23109367 DOI: 10.1002/Anie.201206009 |
0.409 |
|
2012 |
Gruppi F, Liang J, Bartelle BB, Royzen M, Turnbull DH, Canary JW. Supramolecular metal displacement allows on-fluorescence analysis of manganese(II) in living cells. Chemical Communications (Cambridge, England). 48: 10778-80. PMID 23023093 DOI: 10.1039/C2Cc34742C |
0.69 |
|
2012 |
Joyce LA, Canary JW, Anslyn EV. Enantio- and chemoselective differentiation of protected α-amino acids and β-homoamino acids with a single copper(II) host. Chemistry (Weinheim An Der Bergstrasse, Germany). 18: 8064-9. PMID 22592912 DOI: 10.1002/Chem.201103592 |
0.406 |
|
2012 |
Mortezaei S, Catarineu NR, Canary JW. A redox-reconfigurable, ambidextrous asymmetric catalyst. Journal of the American Chemical Society. 134: 8054-7. PMID 22551457 DOI: 10.1021/Ja302283S |
0.751 |
|
2012 |
Canary JW, Dai Z, Mortezaei S. 8.30 Spectroscopic Analysis: Chiroptical Sensors Comprehensive Chirality. 8: 600-624. DOI: 10.1016/B978-0-08-095167-6.00850-8 |
0.737 |
|
2012 |
Canary JW, Dai Z. Dynamic Stereochemistry and Chiroptical Spectroscopy of Metallo-Organic Compounds Comprehensive Chiroptical Spectroscopy. 2: 251-287. DOI: 10.1002/9781118120392.ch7 |
0.392 |
|
2011 |
Joyce LA, Maynor MS, Dragna JM, da Cruz GM, Lynch VM, Canary JW, Anslyn EV. A simple method for the determination of enantiomeric excess and identity of chiral carboxylic acids. Journal of the American Chemical Society. 133: 13746-52. PMID 21780788 DOI: 10.1021/Ja205775G |
0.439 |
|
2011 |
Liang J, Canary JW. A stereodynamic tripodal ligand with three different coordinating arms: synthesis and zinc(II), copper(I) complexation study. Chirality. 23: 24-33. PMID 20222142 DOI: 10.1002/Chir.20833 |
0.498 |
|
2010 |
Liang J, Canary JW. Discrimination between hard metals with soft ligand donor atoms: an on-fluorescence probe for manganese(II). Angewandte Chemie (International Ed. in English). 49: 7710-3. PMID 20821777 DOI: 10.1002/Anie.201002853 |
0.41 |
|
2010 |
Canary JW, Mortezaei S, Liang J. Redox-reconfigurable tripodal coordination complexes: stereodynamic molecular switches. Chemical Communications (Cambridge, England). 46: 5850-60. PMID 20625605 DOI: 10.1039/C0Cc00469C |
0.788 |
|
2010 |
Canary JW, Mortezaei S, Liang J. Transition metal-based chiroptical switches for nanoscale electronics and sensors Coordination Chemistry Reviews. 254: 2249-2266. DOI: 10.1016/J.Ccr.2010.03.004 |
0.765 |
|
2009 |
Liang J, Zhang J, Zhu L, Duarandin A, Young VG, Geacintov N, Canary JW. Structures, metal ion affinities, and fluorescence properties of soluble derivatives of tris((6-phenyl-2-pyridyl)methyl)amine. Inorganic Chemistry. 48: 11196-208. PMID 19877674 DOI: 10.1021/Ic901662Z |
0.548 |
|
2009 |
Dai Z, Khosla N, Canary JW. Visible colour displacement sensing system for manganese(II) Supramolecular Chemistry. 21: 296-300. DOI: 10.1080/10610270802438853 |
0.459 |
|
2008 |
Liu Y, Sha R, Wang R, Ding L, Canary JW, Seeman NC. 2',2'-Ligation Demonstrates the Thermal Dependence of DNA-Directed Positional Control. Tetrahedron. 64: 8417-8422. PMID 19122844 DOI: 10.1016/J.Tet.2008.05.046 |
0.431 |
|
2008 |
Liu Y, Kuzuya A, Sha R, Guillaume J, Wang R, Canary JW, Seeman NC. Coupling across a DNA helical turn yields a hybrid DNA/organic catenane doubly tailed with functional termini. Journal of the American Chemical Society. 130: 10882-3. PMID 18661989 DOI: 10.1021/Ja8041096 |
0.46 |
|
2008 |
Liu Y, Wang R, Ding L, Sha R, Lukeman PS, Canary JW, Seeman NC. Thermodynamic analysis of nylon nucleic acids. Chembiochem : a European Journal of Chemical Biology. 9: 1641-8. PMID 18543259 DOI: 10.1002/Cbic.200800032 |
0.432 |
|
2008 |
Das D, Dai Z, Holmes A, Canary JW. Exploring the scope of redox-triggered chiroptical switches: syntheses, X-ray structures, and circular dichroism of cobalt and nickel complexes of N,N-bis(arylmethyl)methionine derivatives. Chirality. 20: 585-91. PMID 18196593 DOI: 10.1002/Chir.20519 |
0.705 |
|
2008 |
Liu Y, Sha R, Wang R, Ding L, Canary JW, Seeman NC. 2′,2′-Ligation demonstrates the thermal dependence of DNA-directed positional control Tetrahedron. 64: 8417-8422. DOI: 10.1016/j.tet.2008.05.046 |
0.429 |
|
2007 |
Holmes AE, Das D, Canary JW. Chelation-enhanced circular dichroism of tripodal bisporphyrin ligands. Journal of the American Chemical Society. 129: 1506-7. PMID 17243681 DOI: 10.1021/Ja0666147 |
0.614 |
|
2007 |
Dai Z, Canary JW. Tailoring tripodal ligands for zinc sensing New Journal of Chemistry. 31: 1708-1718. DOI: 10.1039/B710803F |
0.495 |
|
2006 |
Zahn S, Das D, Canary JW. Redox-induced ligand reorganization and helicity inversion in copper complexes of N,N-dialkylmethionine derivatives. Inorganic Chemistry. 45: 6056-63. PMID 16842014 DOI: 10.1021/Ic060660Q |
0.599 |
|
2006 |
Anderson EA, Isaacman S, Peabody DS, Wang EY, Canary JW, Kirshenbaum K. Viral nanoparticles donning a paramagnetic coat: conjugation of MRI contrast agents to the MS2 capsid. Nano Letters. 6: 1160-4. PMID 16771573 DOI: 10.1021/Nl060378G |
0.648 |
|
2006 |
Royzen M, Durandin A, Young VG, Geacintov NE, Canary JW. A sensitive probe for the detection of Zn(II) by time-resolved fluorescence. Journal of the American Chemical Society. 128: 3854-5. PMID 16551061 DOI: 10.1021/Ja056631G |
0.674 |
|
2005 |
Barcena HS, Liu B, Mirkin MV, Canary JW. An electrochiroptical molecular switch: mechanistic and kinetic studies. Inorganic Chemistry. 44: 7652-60. PMID 16212392 DOI: 10.1021/Ic051048M |
0.773 |
|
2005 |
Dai Z, Xu X, Canary JW. Rigidified tripodal chiral ligands in the asymmetric recognition of amino compounds. Chirality. 17: S227-33. PMID 15952135 DOI: 10.1002/Chir.20130 |
0.587 |
|
2005 |
Royzen M, Dai Z, Canary JW. Ratiometric displacement approach to Cu(II) sensing by fluorescence. Journal of the American Chemical Society. 127: 1612-3. PMID 15700975 DOI: 10.1021/Ja0431051 |
0.717 |
|
2005 |
Chiu YH, Gabriel GJ, Canary JW. Ternary ligand-zinc-hydroxamate complexes. Inorganic Chemistry. 44: 40-4. PMID 15627358 DOI: 10.1021/ic0493090 |
0.521 |
|
2005 |
Isaacman S, Kumar R, Barco ED, Kent AD, Canary JW, Jerschow A. Critical examination of Fe8 as a contrast agent for magnetic resonance imaging Polyhedron. 24: 2691-2694. DOI: 10.1016/J.Poly.2005.03.138 |
0.656 |
|
2005 |
Holmes AE, Simpson SA, Canary JW. Stereodynamic coordination complexes. Dependence of exciton coupled circular dichroism spectra on molecular conformation and shape Monatshefte Fur Chemie. 136: 461-475. DOI: 10.1007/S00706-005-0285-Z |
0.722 |
|
2004 |
Dai Z, Proni G, Mancheno D, Karimi S, Berova N, Canary JW. Detection of zinc ions by differential circularly polarized fluorescence excitation. Journal of the American Chemical Society. 126: 11760-1. PMID 15382888 DOI: 10.1021/Ja047213Z |
0.436 |
|
2003 |
Zhu L, dos Santos O, Koo CW, Rybstein M, Pape L, Canary JW. Geometry-dependent phosphodiester hydrolysis catalyzed by binuclear copper complexes. Inorganic Chemistry. 42: 7912-20. PMID 14632508 DOI: 10.1021/Ic0340985 |
0.389 |
|
2003 |
Zhu L, Lukeman PS, Canary JW, Seeman NC. Nylon/DNA: Single-stranded DNA with a covalently stitched nylon lining. Journal of the American Chemical Society. 125: 10178-9. PMID 12926933 DOI: 10.1021/Ja035186R |
0.514 |
|
2003 |
Chiu YH, Canary JW. Stability and acidity constants for ternary ligand-zinc-hydroxo complexes of tetradentate tripodal ligands. Inorganic Chemistry. 42: 5107-16. PMID 12924881 DOI: 10.1021/ic025855m |
0.497 |
|
2003 |
Barcena HS, Holmes AE, Zahn S, Canary JW. Redox inversion of helicity in propeller-shaped molecules derived from s-methyl cysteine and methioninol. Organic Letters. 5: 709-11. PMID 12605496 DOI: 10.1021/Ol0275217 |
0.777 |
|
2003 |
Zhang J, Holmes AE, Sharma A, Brooks NR, Rarig RS, Zubieta J, Canary JW. Derivatization, complexation, and absolute configurational assignment of chiral primary amines: application of exciton-coupled circular dichroism. Chirality. 15: 180-9. PMID 12520510 DOI: 10.1002/Chir.10158 |
0.62 |
|
2002 |
Xu X, Maresca KJ, Das D, Zahn S, Zubieta J, Canary JW. Crystal-driven distortion of ligands in copper coordination complexes: conformational pseudo-enantiomers. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 5679-83. PMID 12693049 DOI: 10.1002/1521-3765(20021216)8:24<5679::Aid-Chem5679>3.0.Co;2-A |
0.655 |
|
2002 |
Zhu L, dos Santos O, Seeman NC, Canary JW. Reaction of N3-benzoyl-3',5'-O-(di-tert-butylsilanediyl)uridine with hindered electrophiles: intermolecular N3 to 2'-O protecting group transfer. Nucleosides, Nucleotides & Nucleic Acids. 21: 723-35. PMID 12502286 DOI: 10.1081/Ncn-120015728 |
0.471 |
|
2002 |
Zahn S, Canary JW. Cu(I/II) redox control of molecular conformation and shape in chiral tripodal ligands: binary exciton-coupled circular dichroic states. Journal of the American Chemical Society. 124: 9204-11. PMID 12149026 DOI: 10.1021/Ja0120429 |
0.605 |
|
2002 |
Dai Z, Xu X, Canary JW. Stereochemical control of Zn(II)/Cu(II) selectivity in piperidine tripod ligands. Chemical Communications (Cambridge, England). 1414-5. PMID 12125580 DOI: 10.1039/B111259G |
0.591 |
|
2002 |
Holmes AE, Zahn S, Canary JW. Synthesis and circular dichroism studies of N,N-bis(2-quinolylmethyl)amino acid Cu(II) complexes: determination of absolute configuration and enantiomeric excess by the exciton coupling method. Chirality. 14: 471-7. PMID 12112340 DOI: 10.1002/Chir.10079 |
0.697 |
|
2001 |
Canary JW, Holmes AE, Liu J. Prospects for circular dichroism detection of nonracemic extraterrestrial organic molecules. Enantiomer. 6: 181-8. PMID 11570424 |
0.54 |
|
2001 |
Canary JW, Zahn S. Electronic control of helical chirality. Trends in Biotechnology. 19: 251-5. PMID 11412948 DOI: 10.1016/S0167-7799(01)01664-X |
0.522 |
|
2001 |
Wiskur SL, Lavigne JJ, Ait-Haddou H, Lynch V, Chiu YH, Canary JW, Anslyn EV. pK(a) values and geometries of secondary and tertiary amines complexed to boronic acids-implications for sensor design. Organic Letters. 3: 1311-4. PMID 11348222 DOI: 10.1021/Ol0156805 |
0.604 |
|
2001 |
Zahn S, Proni G, Spada GP, Canary JW. Supramolecular detection of metal ion binding: ligand conformational control of cholesteric induction in nematic liquid crystalline phases. Chemistry (Weinheim An Der Bergstrasse, Germany). 7: 88-93. PMID 11205030 DOI: 10.1002/1521-3765(20010105)7:1<88::Aid-Chem88>3.0.Co;2-0 |
0.579 |
|
2000 |
Canary JW, Zahn S, Chiu YH, dos Santos O, Liu J, Zhu L. Chiroptical switches and sensors based on ligand conformational changes in labile coordination complexes. Enantiomer. 5: 397-403. PMID 11174180 |
0.682 |
|
2000 |
Zahn S, Canary JW. Electron-induced inversion of helical chirality in copper complexes of N,N-dialkylmethionines. Science (New York, N.Y.). 288: 1404-7. PMID 10827947 DOI: 10.1126/Science.288.5470.1404 |
0.603 |
|
2000 |
Zahn S, Canary JW. Redox control of stilbylvinylpyridine chormophore pairwise orientations: Towards solid state materials for molecular electronics Materials Research Society Symposium - Proceedings. 598: BB3.19.1-BB3.19.5. DOI: 10.1557/Proc-598-Bb3.19 |
0.492 |
|
1999 |
Zahn S, Canary JW. Absolute configurations of N,N-dialkyl alpha-amino acids and beta-amino alcohols from exciton-coupled circular dichroism spectra of Cu(II) complexes. Organic Letters. 1: 861-4. PMID 10823214 DOI: 10.1021/Ol990715A |
0.555 |
|
1999 |
Chiu YH, Dos Santos O, Canary JW. Conformational control of propeller-like chirality in Zn(II) complexes: Tightly balanced steric bias Tetrahedron. 55: 12069-12078. DOI: 10.1016/S0040-4020(99)00713-9 |
0.539 |
|
1998 |
Zahn S, Canary JW. Redox-Switched Exciton-Coupled Circular Dichroism: A Novel Strategy for Binary Molecular Switching. Angewandte Chemie (International Ed. in English). 37: 305-307. PMID 29711262 DOI: 10.1002/(Sici)1521-3773(19980216)37:3<305::Aid-Anie305>3.0.Co;2-T |
0.558 |
|
1998 |
Xu X, Allen CS, Chuang C, Canary JW. A tetrahedral zinc(II) complex of tris(2-pyridylethyl)amine. Acta Crystallographica. Section C, Crystal Structure Communications. 54: 600-1. PMID 9636993 DOI: 10.1107/S0108270197017733 |
0.465 |
|
1998 |
Canary JW, Allen CS, Castagnetto JM, Chiu YH, Toscano PJ, Wang Y. Solid State and Solution Characterization of Chiral, Conformationally Mobile Tripodal Ligands Inorganic Chemistry. 37: 6255-6262. DOI: 10.1021/Ic9803098 |
0.514 |
|
1998 |
Zahn S, Canary J. Redoxschaltbarer, excitonengekoppelter Circulardichroismus: eine neue Strategie für die Entwicklung molekularer Schalter Angewandte Chemie. 110: 321-323. DOI: 10.1002/(Sici)1521-3757(19980202)110:3<321::Aid-Ange321>3.0.Co;2-E |
0.456 |
|
1998 |
Zahn S, Canary JW. Redox-switched exciton-coupled circular dichroism: A novel strategy for binary molecular switching Angewandte Chemie - International Edition in English. 37: 305-307. |
0.506 |
|
1997 |
Chuang CL, dos Santos O, Xu X, Canary JW. Synthesis and Cyclic Voltammetry Studies of Copper Complexes of Bromo- and Alkoxyphenyl-Substituted Derivatives of Tris(2-pyridylmethyl)amine: Influence of Cation-Alkoxy Interactions on Copper Redox Potentials. Inorganic Chemistry. 36: 1967-1972. PMID 11669805 DOI: 10.1021/Ic960942Y |
0.489 |
|
1997 |
Castagnetto JM, Xu X, Berova ND, Canary JW. Absolute configurational assignment of self-organizing asymmetric tripodal ligand-metal complexes. Chirality. 9: 616-22. PMID 9329182 DOI: 10.1002/(Sici)1520-636X(1997)9:5/6<616::Aid-Chir32>3.0.Co;2-P |
0.487 |
|
1990 |
Breslow R, Canary JW, Varney M, Waddell ST, Yang D. Artificial transminases linking pyridoxamine to binding cavities: Controlling the geometry Journal of the American Chemical Society. 112: 5212-5219. DOI: 10.1021/Ja00169A032 |
0.371 |
|
1987 |
Doxsee KM, Feigel M, Stewart KD, Canary JW, Knobler CB, Cram DJ. Host-guest complexation. 42. Preorganization strongly enhances the tendency of hemispherands to form hemispheraplexes Journal of the American Chemical Society. 109: 3098-3107. DOI: 10.1021/Ja00244A037 |
0.645 |
|
Low-probability matches (unlikely to be authored by this person) |
1997 |
Canary JW, Gibb BC. Selective recognition of organic molecules by metallohosts Progress in Inorganic Chemistry. 45: 1-81. DOI: 10.1002/9780470166468.Ch1 |
0.297 |
|
2006 |
Zhang J, Canary JW. Redox-triggered interconversion between piperidine chair conformations in a Cu(I/II) complex. Organic Letters. 8: 3907-10. PMID 16928035 DOI: 10.1021/ol061364k |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Chuang C, Lim K, Canary JW. The influence of phenyl substituents on the redox potentials of sterically hindered tripodal ligand/copper complexes Supramolecular Chemistry. 5: 39-43. DOI: 10.1080/10610279508029886 |
0.255 |
|
1995 |
Canary JW, Allen CS, Castagnetto JM, Wang Y. Conformationally driven, propeller-like chirality in labile coordination complexes Journal of the American Chemical Society. 117: 8484-8485. |
0.232 |
|
1995 |
Chuang CL, Lim K, Chen Q, Zubieta J, Canary JW. Synthesis, cyclic voltammetry, and X-ray crystal structures of copper(I) and copper(II) complexes of tris((6-phenyl-2-pyridyl)methyl)amine (TPPA) Inorganic Chemistry. 34: 2562-2568. |
0.228 |
|
1997 |
Chuang CL, Dos Santos O, Xu X, Canary JW. Synthesis and Cyclic Voltammetry Studies of Copper Complexes of Bromo- and Alkoxyphenyl-Substituted Derivatives of Tris(2-pyridylmethyl)amine: Influence of Cation - Alkoxy Interactions on Copper Redox Potentials Inorganic Chemistry. 36: 1967-1972. |
0.222 |
|
2005 |
Zhang J, Siu K, Lin CH, Canary JW. Conformational dynamics of Cu(I) complexes of tripodal ligands: Steric control of molecular motion New Journal of Chemistry. 29: 1147-1151. DOI: 10.1039/b509050d |
0.221 |
|
2015 |
Zhang Y, Basu K, Canary JW, Jerschow A. Singlet lifetime measurements in an all-proton chemically equivalent spin system by hyperpolarization and weak spin lock transfers. Physical Chemistry Chemical Physics : Pccp. 17: 24370-5. PMID 26330001 DOI: 10.1039/C5Cp03716F |
0.218 |
|
1995 |
Chuang CL, Frid M, Canary JW. Geometric control of selectivity in alkali metal ion complexation by acyclic N4-tripodal ligands Tetrahedron Letters. 36: 2909-2912. DOI: 10.1016/0040-4039(95)00464-N |
0.217 |
|
2003 |
Maverick EF, Knobler CB, Khan S, Canary JW, Dicker IB, Trueblood KN. Torsional motion in (tert-butyl)ammonium hemispheraplexes: Rotational barriers and energy of binding Helvetica Chimica Acta. 86: 1309-1319. DOI: 10.1002/Hlca.200390119 |
0.189 |
|
1999 |
Caulton KG, Xu X, Lajmi AR, Canary JW, Brand U, Rombach M, Vahrenkamp H. Acetaldehyde hydration by zinc-hydroxo complexes: Coordination number expansion during catalysis. Methylation of zinc bound thiolates: A model for cobalamine independent methionine synthase Chemtracts. 12: 890-894. |
0.188 |
|
2009 |
Canary JW. Redox-triggered chiroptical molecular switches. Chemical Society Reviews. 38: 747-56. PMID 19322467 DOI: 10.1039/b800412a |
0.179 |
|
1995 |
Canary JW, Xu J, Castagnetto JM, Rentzeperis D, Marky LA. Enthalpic control of zinc-water acidity in complexes of tris(2-aminoethyl)amine and tris(2-(dimethylamino)ethyl)amine Journal of the American Chemical Society. 117: 11545-11547. |
0.172 |
|
2008 |
Matile S, Canary J, Harada EN, Caldwell J. Special issue honoring professor Nina Berova Chirality. 20: 249-250. DOI: 10.1002/Chir.20497 |
0.172 |
|
1995 |
Allen CS, Chuang CL, Cornebise M, Canary JW. Electrospray mass spectrometry and X-ray crystallography studies of divalent metal ion complexes of tris (2-pyridylmethyl) amine Inorganica Chimica Acta. 239: 29-37. DOI: 10.1016/0020-1693(95)04710-7 |
0.167 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
1993 |
Canary J, Chuang C, Lim K, Chen Q, Zubieta J. Synthesis, cyclic voltammetry, and X-ray structures of [CU(TPPA)]BPH4 and [CU(TPPA)(MECN)](CLO4)2 (TPPA = Tris(6-phenyl-2-pyridylmethyl)amine). Journal of Inorganic Biochemistry. 51: 67. DOI: 10.1016/0162-0134(93)85103-F |
0.162 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Combining aminocyanine dyes with polyamide dendrons: a promising strategy for imaging in the near-infrared region. Chemistry (Weinheim An Der Bergstrasse, Germany). 17: 3619-29. PMID 21337432 DOI: 10.1002/Chem.201002268 |
0.161 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
1992 |
Canary JW, Chuang C, Cornebise M, Lim K, Xu J. Characterization of biomimetic coordination complexes and metalloproteins by electrospray mass spectrometry. Journal of Inorganic Biochemistry. 47: 46. DOI: 10.1016/0162-0134(92)84118-7 |
0.157 |
|
2005 |
Zhang J, Albelda MT, Liu Y, Canary JW. Chiral nanotechnology. Chirality. 17: 404-20. PMID 15991226 DOI: 10.1002/chir.20178 |
0.152 |
|
1997 |
Dos Santos O, Lajmi AR, Canary JW. Synthesis of a dinucleating ligand with addressed ion binding sites Tetrahedron Letters. 38: 4383-4386. DOI: 10.1016/S0040-4039(97)00937-4 |
0.152 |
|
2016 |
Zhang Y, Duan X, Soon PC, Sychrovský V, Canary JW, Jerschow A. Limits in Proton Nuclear Singlet-State Lifetimes Measured with para-Hydrogen-Induced Polarization. Chemphyschem : a European Journal of Chemical Physics and Physical Chemistry. PMID 27460052 DOI: 10.1002/Cphc.201600663 |
0.122 |
|
1996 |
Chen Y, Bannwart RS, Canary JW. Synthesis and characterization of polycarbazim, a novel polvaniline derivative American Chemical Society, Polymer Preprints, Division of Polymer Chemistry. 37: 335-336. |
0.119 |
|
2022 |
Kharkov B, Duan X, Rantaharju J, Sabba M, Levitt MH, Canary JW, Jerschow A. Weak nuclear spin singlet relaxation mechanisms revealed by experiment and computation. Physical Chemistry Chemical Physics : Pccp. 24: 7531-7538. PMID 35290424 DOI: 10.1039/d1cp05537b |
0.118 |
|
1991 |
Breslow R, Canary JW. Rapid nucleophilic substitutions on cyclopentadienyl iodide and bromide Journal of the American Chemical Society. 113: 3950-3951. |
0.104 |
|
2021 |
Chen S, Vurusaner B, Pena S, Thu CT, Mahal LK, Fisher EA, Canary JW. Two-Photon, Ratiometric, Quantitative Fluorescent Probe Reveals Fluctuation of Peroxynitrite Regulated by Arginase 1. Analytical Chemistry. PMID 34269045 DOI: 10.1021/acs.analchem.1c00911 |
0.102 |
|
2014 |
Zhang Y, Soon PC, Jerschow A, Canary JW. Long-lived ¹H nuclear spin singlet in dimethyl maleate revealed by addition of thiols. Angewandte Chemie (International Ed. in English). 53: 3396-9. PMID 24623618 DOI: 10.1002/Anie.201310284 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2008 |
Canary JW. Book Review of Dynamic Stereochemistry of Chiral Compounds: Principles and Applications Dynamic Stereochemistry of Chiral Compounds: Principles and Applications . By Christian Wolf (Georgetown University, Washington, DC). Royal Society of Chemistry: Cambridge. 2008. xx + 512 pp. $99.00. ISBN 978-0-85404-246-3 . Journal of the American Chemical Society. 130: 15219-15220. DOI: 10.1021/ja8074055 |
0.1 |
|
2005 |
Berova N, Canary JW, Welch CJ. The sixteenth International Symposium on Chiral Discrimination (ISCD-16): July 2004 Chirality. 17: iv. DOI: 10.1002/Chir.20163 |
0.1 |
|
2019 |
Kharkov B, Duan X, Tovar ES, Canary JW, Jerschow A. Singlet excitation in the intermediate magnetic equivalence regime and field-dependent study of singlet-triplet leakage. Physical Chemistry Chemical Physics : Pccp. PMID 30657502 DOI: 10.1039/C8Cp06883F |
0.099 |
|
1997 |
Xu J, Chuang CL, Canary JW. Synthesis of tris((3-isoquinolyl)methyl)amine and bis((2-pyridyl)methyl)-(3-isoquinolyl)methylamine Inorganica Chimica Acta. 256: 125-128. |
0.092 |
|
1990 |
Stevens RV, Canary JW. Synthesis of 2-octalones from quinaldine Journal of Organic Chemistry. 55: 2237-2240. DOI: 10.1021/Jo00294A049 |
0.085 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1997 |
Canary JW. Electronic Conference on Trends in Organic Chemistry: ECTOC-1/CD-ROM. June 12−July 7, 1995 Edited by Henry S. Rzepa, Christopher Leach, and Jonathan M. Goodman. The Royal Society of Chemistry: Cambridge, 1996. £50.00. ISBN 0-85404-8995. Journal of the American Chemical Society. 119: 4567-4567. DOI: 10.1021/ja9659232 |
0.084 |
|
1998 |
Canary JW, Wang Y, Roy R, Que L, Miyake H. Tris[(2-pyridyl)methyl]amine (TPA) and (+)-Bis[(2-pyridyl)methyl]-1-(2- pyridyl)-ethylamine (α-metpa) Inorganic Syntheses. 32: 70-75. |
0.083 |
|
2017 |
Kharkov B, Duan X, Canary JW, Jerschow A. Effect of convection and B1 inhomogeneity on singlet relaxation experiments. Journal of Magnetic Resonance (San Diego, Calif. : 1997). 284: 1-7. PMID 28926738 DOI: 10.1016/J.Jmr.2017.09.005 |
0.077 |
|
2017 |
Kharkov B, Duan X, Canary JW, Jerschow A. Effect of convection and B1 inhomogeneity on singlet relaxation experiments. Journal of Magnetic Resonance (San Diego, Calif. : 1997). 284: 1-7. PMID 28926738 DOI: 10.1016/J.Jmr.2017.09.005 |
0.077 |
|
2017 |
Kharkov B, Duan X, Canary JW, Jerschow A. Effect of convection and B1 inhomogeneity on singlet relaxation experiments. Journal of Magnetic Resonance (San Diego, Calif. : 1997). 284: 1-7. PMID 28926738 DOI: 10.1016/J.Jmr.2017.09.005 |
0.077 |
|
2017 |
Kharkov B, Duan X, Canary JW, Jerschow A. Effect of convection and B1 inhomogeneity on singlet relaxation experiments. Journal of Magnetic Resonance (San Diego, Calif. : 1997). 284: 1-7. PMID 28926738 DOI: 10.1016/J.Jmr.2017.09.005 |
0.077 |
|
1998 |
Castagnetto JM, Canary JW. A chiroptically enhanced fluorescent chemosensor Chemical Communications. 203-204. |
0.075 |
|
2013 |
Soon PC, Xu X, Zhang B, Gruppi F, Canary JW, Jerschow A. Hyperpolarization of amino acid precursors to neurotransmitters with parahydrogen induced polarization. Chemical Communications (Cambridge, England). 49: 5304-6. PMID 23648773 DOI: 10.1039/C3Cc40426A |
0.074 |
|
1995 |
Moriarty RM, Enache LA, Kinney WA, Allen CS, Canary JW, Tuladhar SM, Guo L. Stereoselective synthesis of squalamine dessulfate Tetrahedron Letters. 36: 5139-5142. DOI: 10.1016/0040-4039(95)01011-6 |
0.073 |
|
2011 |
Tang JA, Gruppi F, Fleysher R, Sodickson DK, Canary JW, Jerschow A. Extended para-hydrogenation monitored by NMR spectroscopy. Chemical Communications (Cambridge, England). 47: 958-60. PMID 21079839 DOI: 10.1039/C0Cc03421E |
0.073 |
|
1985 |
Reiser S, Smith JC, Mertz W, Holbrook JT, Scholfield DJ, Powell AS, Canfield WK, Canary JJ. Indices of copper status in humans consuming a typical American diet containing either fructose or starch. The American Journal of Clinical Nutrition. 42: 242-51. PMID 4025196 |
0.072 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2002 |
Canary J. Molecular Switches edited by Ben L. Feringa Advanced Synthesis & Catalysis. 344: 563. DOI: 10.1002/1615-4169(200207)344:5<563::AID-ADSC563>3.0.CO;2-M |
0.069 |
|
2007 |
Angelo NG, Henchey LK, Waxman AJ, Canary JW, Arora PS, Wink D. Synthesis and characterization of aldol condensation products from unknown aldehydes and ketones. An inquiry-based experiment in the undergraduate laboratory Journal of Chemical Education. 84: 1816-1818. DOI: 10.1021/Ed084P1816 |
0.066 |
|
1994 |
Aliprantis AO, Canary JW. Observation of catalytic intermediates in the Suzuki reaction by electrospray mass spectrometry Journal of the American Chemical Society. 116: 6985-6986. DOI: 10.1021/Ja00094A083 |
0.064 |
|
1986 |
Reiser S, Hallfrisch J, Fields M, Powell A, Mertz W, Prather ES, Canary JJ. Effects of sugars on indices of glucose tolerance in humans. The American Journal of Clinical Nutrition. 43: 151-9. PMID 3002162 |
0.059 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/Chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
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2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2013 |
Arora PS, Canary JW. Organic Chemistry: Principles in Context. A Story Telling Historical Approach, by Mark M. Green. ISBN: 0615702716 Chirality. 25: 582-582. DOI: 10.1002/chir.22167 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/Chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
2011 |
Ornelas C, Lodescar R, Durandin A, Canary JW, Pennell R, Liebes LF, Weck M. Inside Cover: Combining Aminocyanine Dyes with Polyamide Dendrons: A Promising Strategy for Imaging in the Near‐Infrared Region (Chem. Eur. J. 13/2011) Chemistry – a European Journal. 17: 3526-3526. DOI: 10.1002/chem.201190061 |
0.058 |
|
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