| Year |
Citation |
Score |
| 2023 |
Xu M, Ma X, Pigga JE, Zhang H, Wang S, Zhao W, Deng H, Wu AM, Liu R, Wu Z, Fox JM, Li Z. Development of F-Labeled hydrophilic -cyclooctene as a bioorthogonal tool for PET probe construction. Chemical Communications (Cambridge, England). PMID 37877355 DOI: 10.1039/d3cc04212j |
0.772 |
|
| 2022 |
Jemas A, Xie Y, Pigga JE, Caplan JL, Am Ende CW, Fox JM. Catalytic Activation of Bioorthogonal Chemistry with Light (CABL) Enables Rapid, Spatiotemporally Controlled Labeling and No-Wash, Subcellular 3D-Patterning in Live Cells Using Long Wavelength Light. Journal of the American Chemical Society. PMID 35072462 DOI: 10.1021/jacs.1c10390 |
0.752 |
|
| 2021 |
Fox JM, Pigga JE, Rosenberger JE, Jemas A, Boyd SJ, Dmitrenko O, Xie Y. General, Divergent Platform for Diastereoselective Synthesis of trans-Cyclooctenes with High Reactivity and Favorable Physiochemical Properties. Angewandte Chemie (International Ed. in English). PMID 33742526 DOI: 10.1002/anie.202101483 |
0.808 |
|
| 2020 |
Pigga JE, Fox JM. Flow Photochemical Syntheses of -Cyclooctenes and -Cycloheptenes Driven by Metal Complexation. Israel Journal of Chemistry. 60: 207-218. PMID 34108738 DOI: 10.1002/ijch.201900085 |
0.787 |
|
| 2020 |
Fox JM, Xie Y, Fang Y, Huang Z, Tallon A, Am Ende C. Divergent Synthesis of Monosubstituted and Unsymmetrical 3,6-Disubstituted Tetrazines from Carboxylic Ester Precursors. Angewandte Chemie (International Ed. in English). PMID 32559350 DOI: 10.1002/anie.202005569 |
0.326 |
|
| 2020 |
Feng H, Zhang H, Wang M, Vannam R, Wang H, Yan X, Ouyang W, Jia X, Fox J, Li Z. Improving Tumor-to-Background Contrast Through Hydrophilic Tetrazines: The Construction of 18F Labeled PET Agents Targeting Non-Small Cell Lung Carcinoma. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32030822 DOI: 10.1002/Chem.202000028 |
0.339 |
|
| 2020 |
Xie Y, Fang Y, Huang Z, Tallon AM, Ende CWa, Fox JM. Divergent Synthesis of Monosubstituted and Unsymmetrical 3,6‐Disubstituted Tetrazines from Carboxylic Ester Precursors Angewandte Chemie. 59: 16967-16973. DOI: 10.1002/Ange.202005569 |
0.433 |
|
| 2019 |
Fang Y, Judkins JC, Boyd SJ, Am Ende CW, Rohlfing K, Huang Z, Xie Y, Johnson DS, Fox JM. Studies on the Stability and Stabilization of Cyclooctenes through Radical Inhibition and Silver (I) Metal Complexation. Tetrahedron. 75: 4307-4317. PMID 32612312 DOI: 10.1016/J.Tet.2019.05.038 |
0.35 |
|
| 2019 |
Lambert W, Fang Y, Mahapatra S, Huang Z, Am Ende CW, Fox JM. Installation of Minimal Tetrazines Through Silver-mediated Liebeskind-Srogl Coupling with Arylboronic Acids. Journal of the American Chemical Society. PMID 31603679 DOI: 10.1021/Jacs.9B08677 |
0.375 |
|
| 2019 |
Scinto SL, Ekanayake O, Seneviratne UI, Pigga JE, Brannick SJ, Taylor MT, Liu J, Am Ende CW, Rozovsky S, Fox JM. Dual-Reactivity trans-Cyclooctenol Probes for Sulfenylation in Live Cells Enable Temporal Control via Bioorthogonal Quenching. Journal of the American Chemical Society. PMID 31246462 DOI: 10.1021/Jacs.9B01164 |
0.767 |
|
| 2018 |
Liu S, Moore AC, Zerdoum AB, Zhang H, Scinto SL, Zhang H, Gong L, Burris DL, Rajasekaran AK, Fox JM, Jia X. Cellular interactions with hydrogel microfibers synthesized via interfacial tetrazine ligation. Biomaterials. 180: 24-35. PMID 30014964 DOI: 10.1016/J.Biomaterials.2018.06.042 |
0.302 |
|
| 2018 |
Fang Y, Zhang H, Huang Z, Scinto SL, Yang JC, Am Ende CW, Dmitrenko O, Johnson DS, Fox JM. Photochemical syntheses, transformations, and bioorthogonal chemistry of -cycloheptene and sila -cycloheptene Ag(i) complexes. Chemical Science. 9: 1953-1963. PMID 29675242 DOI: 10.1039/C7Sc04773H |
0.352 |
|
| 2018 |
Smith NJ, Rohlfing K, Sawicki LA, Kharkar PM, Boyd SJ, Kloxin AM, Fox JM. Fast, irreversible modification of cysteines through strain releasing conjugate additions of cyclopropenyl ketones. Organic & Biomolecular Chemistry. PMID 29521395 DOI: 10.1039/C8Ob00166A |
0.667 |
|
| 2018 |
Darko A, Fox J, Boyd S. Large-Scale Flow Photochemical Synthesis of Functionalized trans-Cyclooctenes Using Sulfonated Silica Gel Synthesis. 50: 4875-4882. DOI: 10.1055/S-0037-1610240 |
0.359 |
|
| 2017 |
O'Brien JGK, Chintala SR, Fox JM. Stereoselective Synthesis of Bicyclo[6.1.0]nonene Precursors of the Bioorthogonal Reagents s-TCO and BCN. The Journal of Organic Chemistry. PMID 29171257 DOI: 10.1021/Acs.Joc.7B02329 |
0.405 |
|
| 2017 |
Lambert WD, Scinto SL, Dmitrenko O, Boyd SJ, Magboo R, Mehl RA, Chin JW, Fox JM, Wallace S. Computationally guided discovery of a reactive, hydrophilic trans-5-oxocene dienophile for bioorthogonal labeling. Organic & Biomolecular Chemistry. PMID 28752889 DOI: 10.1039/C7Ob01707C |
0.416 |
|
| 2017 |
Shaw JT, Lamb KN, Squitieri RA, Chintala SR, Kwong AJ, Balmond EI, Soldi C, Dmytrenko O, Reis MC, Chung R, Addison JB, Fettinger JC, Hein JC, Tantillo DJ, Fox JM. Synthesis of Benzodihydrofurans by Asymmetric C-H Insertion Reactions of Donor/Donor Carbenoids. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28544228 DOI: 10.1002/Chem.201701630 |
0.45 |
|
| 2016 |
Wang M, Svatunek D, Rohlfing K, Liu Y, Wang H, Giglio B, Yuan H, Wu Z, Li Z, Fox J. Conformationally Strained trans-Cyclooctene (sTCO) Enables the Rapid Construction of (18)F-PET Probes via Tetrazine Ligation. Theranostics. 6: 887-95. PMID 27162558 DOI: 10.7150/Thno.14742 |
0.696 |
|
| 2016 |
Panish RA, Chintala SR, Fox JM. Mixed-Ligand Chiral Rhodium(II) Catalyst Enables the Enantioselective Total Synthesis of Piperarborenine B. Angewandte Chemie (International Ed. in English). PMID 26991451 DOI: 10.1002/Anie.201600766 |
0.808 |
|
| 2016 |
Bayat M, Fox JM. An Efficient One-Pot Synthesis of Bis Butenolides Journal of Heterocyclic Chemistry. 53: 1661-1664. DOI: 10.1002/Jhet.2469 |
0.439 |
|
| 2015 |
DeAngelis A, Panish R, Fox JM. Rh-Catalyzed Intermolecular Reactions of α-Alkyl-α-Diazo Carbonyl Compounds with Selectivity over β-Hydride Migration. Accounts of Chemical Research. PMID 26689221 DOI: 10.1021/Acs.Accounts.5B00425 |
0.79 |
|
| 2015 |
Murrey HE, Judkins JC, Am Ende CW, Ballard TE, Fang Y, Riccardi K, Di L, Guilmette ER, Schwartz JW, Fox JM, Johnson DS. Systematic Evaluation of Bioorthogonal Reactions in Live Cells with Clickable HaloTag Ligands: Implications for Intracellular Imaging. Journal of the American Chemical Society. 137: 11461-75. PMID 26270632 DOI: 10.1021/Jacs.5B06847 |
0.392 |
|
| 2015 |
Panish R, Selvaraj R, Fox JM. Rh(II)-Catalyzed Reactions of Diazoesters with Organozinc Reagents. Organic Letters. PMID 26241081 DOI: 10.1021/Acs.Orglett.5B01836 |
0.821 |
|
| 2015 |
Taylor MT, Fox JM. Biosynthesis of the C15-acetogenin laurepoxide may involve bromine-induced skeletal rearrangement of a Δ4-oxocene precursor. Tetrahedron Letters. 56: 3560-3563. PMID 26146420 DOI: 10.1016/J.Tetlet.2015.03.009 |
0.315 |
|
| 2015 |
Selvaraj R, Giglio B, Liu S, Wang H, Wang M, Yuan H, Chintala SR, Yap LP, Conti PS, Fox JM, Li Z. Improved metabolic stability for 18F PET probes rapidly constructed via tetrazine trans-cyclooctene ligation. Bioconjugate Chemistry. 26: 435-42. PMID 25679331 DOI: 10.1021/Acs.Bioconjchem.5B00089 |
0.576 |
|
| 2014 |
Selvaraj R, Fox JM. An efficient and mild oxidant for the synthesis of s-tetrazines. Tetrahedron Letters. 55: 4795-4797. PMID 26146418 DOI: 10.1016/J.Tetlet.2014.07.012 |
0.589 |
|
| 2014 |
Darko A, Wallace S, Dmitrenko O, Machovina MM, Mehl RA, Chin JW, Fox JM. Conformationally Strained trans-Cyclooctene with Improved Stability and Excellent Reactivity in Tetrazine Ligation. Chemical Science. 5: 3770-3776. PMID 26113970 DOI: 10.1039/C4Sc01348D |
0.335 |
|
| 2014 |
Selvaraj R, Fox JM. An efficient and mild oxidant for the synthesis of s-tetrazines Tetrahedron Letters. 4795-4797. DOI: 10.1016/j.tetlet.2014.07.012 |
0.518 |
|
| 2014 |
Selvaraj R, Chintala SR, Taylor MT, Fox JM. 3‐Hydroxymethyl‐3‐phenylcyclopropene Organic Syntheses. 91: 322-337. DOI: 10.1002/0471264229.Os091.28 |
0.646 |
|
| 2013 |
Selvaraj R, Fox JM. trans-Cyclooctene--a stable, voracious dienophile for bioorthogonal labeling. Current Opinion in Chemical Biology. 17: 753-60. PMID 23978373 DOI: 10.1016/J.Cbpa.2013.07.031 |
0.589 |
|
| 2013 |
Panish R, Chintala SR, Boruta DT, Fang Y, Taylor MT, Fox JM. Enantioselective synthesis of cyclobutanes via sequential Rh-catalyzed bicyclobutanation/Cu-catalyzed homoconjugate addition. Journal of the American Chemical Society. 135: 9283-6. PMID 23758288 DOI: 10.1021/Ja403811T |
0.801 |
|
| 2013 |
Xie X, Li Y, Fox JM. Selective syntheses of Δ(α,β) and Δ(β,γ) butenolides from allylic cyclopropenecarboxylates via tandem ring expansion/[3,3]-sigmatropic rearrangements. Organic Letters. 15: 1500-3. PMID 23514430 DOI: 10.1021/Ol400264A |
0.571 |
|
| 2013 |
Fisher LA, Smith NJ, Fox JM. Chiral cyclopropenyl ketones: reactive and selective Diels-Alder dienophiles. The Journal of Organic Chemistry. 78: 3342-8. PMID 23438063 DOI: 10.1021/Jo302683T |
0.777 |
|
| 2013 |
Liu S, Hassink M, Selvaraj R, Yap LP, Park R, Wang H, Chen X, Fox JM, Li Z, Conti PS. Efficient 18F labeling of cysteine-containing peptides and proteins using tetrazine-trans-cyclooctene ligation. Molecular Imaging. 12: 121-8. PMID 23415400 DOI: 10.2310/7290.2012.00013 |
0.779 |
|
| 2013 |
Wu Z, Liu S, Hassink M, Nair I, Park R, Li L, Todorov I, Fox JM, Li Z, Shively JE, Conti PS, Kandeel F. Development and evaluation of 18F-TTCO-Cys40-Exendin-4: a PET probe for imaging transplanted islets. Journal of Nuclear Medicine : Official Publication, Society of Nuclear Medicine. 54: 244-51. PMID 23297075 DOI: 10.2967/Jnumed.112.109694 |
0.751 |
|
| 2013 |
Xie X, Fox JM. Diastereoselective syntheses of highly substituted methylenecyclopropanes via copper- or iron-catalyzed reactions of 1,2-disubstituted 3-(hydroxymethyl)cyclopropenes with grignard reagents Synthesis (Germany). 45: 1807-1814. DOI: 10.1055/S-0033-1338876 |
0.62 |
|
| 2012 |
Boruta DT, Dmitrenko O, Yap GP, Fox JM. Rh(2)(S-PTTL)(3)TPA-A Mixed Ligand Dirhodium(II) Catalyst for Enantioselective Reactions of α-Alkyl-α-Diazoesters. Chemical Science (Royal Society of Chemistry : 2010). 3: 1589-1593. PMID 23125912 DOI: 10.1039/C2Sc01134D |
0.801 |
|
| 2012 |
Hassink MD, Fox JM. Functionalized Cyclopropenes and Methylenecyclopropenes from Dianions of 3-Hydroxymethylcyclopropenes. Synthesis. 44: 2843-2850. PMID 23125466 DOI: 10.1055/S-0031-1290822 |
0.81 |
|
| 2012 |
Tarwade V, Selvaraj R, Fox JM. Facially selective Cu-catalyzed carbozincation of cyclopropenes using arylzinc reagents formed by sequential I/Mg/Zn exchange. The Journal of Organic Chemistry. 77: 9900-4. PMID 23035947 DOI: 10.1021/Jo3019076 |
0.779 |
|
| 2012 |
Lang K, Davis L, Wallace S, Mahesh M, Cox DJ, Blackman ML, Fox JM, Chin JW. Genetic Encoding of bicyclononynes and trans-cyclooctenes for site-specific protein labeling in vitro and in live mammalian cells via rapid fluorogenic Diels-Alder reactions. Journal of the American Chemical Society. 134: 10317-20. PMID 22694658 DOI: 10.1021/Ja302832G |
0.787 |
|
| 2012 |
DeAngelis A, Dmitrenko O, Fox JM. Rh-catalyzed intermolecular reactions of cyclic α-diazocarbonyl compounds with selectivity over tertiary C-H bond migration. Journal of the American Chemical Society. 134: 11035-43. PMID 22676258 DOI: 10.1021/Ja3046712 |
0.821 |
|
| 2012 |
Seitchik JL, Peeler JC, Taylor MT, Blackman ML, Rhoads TW, Cooley RB, Refakis C, Fox JM, Mehl RA. Genetically encoded tetrazine amino acid directs rapid site-specific in vivo bioorthogonal ligation with trans-cyclooctenes. Journal of the American Chemical Society. 134: 2898-901. PMID 22283158 DOI: 10.1021/Ja2109745 |
0.786 |
|
| 2012 |
Liu DS, Tangpeerachaikul A, Selvaraj R, Taylor MT, Fox JM, Ting AY. Diels-Alder cycloaddition for fluorophore targeting to specific proteins inside living cells. Journal of the American Chemical Society. 134: 792-5. PMID 22176354 DOI: 10.1021/Ja209325N |
0.573 |
|
| 2012 |
Li Z, Liu S, Hassink M, Selvaraj R, Yap L, Chen X, Fox JM, Conti PS. Abstract 370: Tetrazine trans-cyclooctene ligation: An efficient18F labeling method for cysteine containing peptides and proteins Cancer Research. 72: 370-370. DOI: 10.1158/1538-7445.Am2012-370 |
0.59 |
|
| 2012 |
Boruta DT, Dmitrenko O, Yap GPA, Fox JM. ChemInform Abstract: Rh2(S-PTTL)3TPA - A Mixed-Ligand Dirhodium(II) Catalyst for Enantioselective Reactions of α-Alkyl-α-diazoesters. Cheminform. 43: no-no. DOI: 10.1002/chin.201238026 |
0.778 |
|
| 2011 |
Royzen M, Taylor MT, Deangelis A, Fox JM. Total Synthesis of Hyacinthacine A2: Stereocontrolled 5-aza-cyclooctene Photoisomerization and Transannular Hydroamination with Planar-to-Point Chirality Transfer. Chemical Science (Royal Society of Chemistry : 2010). 2: 2162-2165. PMID 23125911 DOI: 10.1039/C1Sc00442E |
0.801 |
|
| 2011 |
Selvaraj R, Liu S, Hassink M, Huang CW, Yap LP, Park R, Fox JM, Li Z, Conti PS. Tetrazine-trans-cyclooctene ligation for the rapid construction of integrin αvβ₃ targeted PET tracer based on a cyclic RGD peptide. Bioorganic & Medicinal Chemistry Letters. 21: 5011-4. PMID 21601452 DOI: 10.1016/J.Bmcl.2011.04.116 |
0.787 |
|
| 2011 |
Taylor MT, Blackman ML, Dmitrenko O, Fox JM. Design and synthesis of highly reactive dienophiles for the tetrazine-trans-cyclooctene ligation. Journal of the American Chemical Society. 133: 9646-9. PMID 21599005 DOI: 10.1021/Ja201844C |
0.772 |
|
| 2011 |
Hassink M, Liu X, Fox JM. Copper-catalyzed synthesis of 2,4-disubstituted allenoates from α-diazoesters. Organic Letters. 13: 2388-91. PMID 21486078 DOI: 10.1021/Ol2006242 |
0.796 |
|
| 2011 |
Dong Z, Bai S, Yap GP, Fox JM. Interplay between the diamine structure and absolute helicity in Ni-salen metallofoldamers. Chemical Communications (Cambridge, England). 47: 3781-3. PMID 21298140 DOI: 10.1039/C0Cc04794E |
0.547 |
|
| 2011 |
DeAngelis A, Shurtleff VW, Dmitrenko O, Fox JM. Rhodium(II)-catalyzed enantioselective C-H functionalization of indoles. Journal of the American Chemical Society. 133: 1650-3. PMID 21265565 DOI: 10.1021/Ja1093309 |
0.806 |
|
| 2010 |
Li Z, Cai H, Hassink M, Blackman ML, Brown RC, Conti PS, Fox JM. Tetrazine-trans-cyclooctene ligation for the rapid construction of 18F labeled probes. Chemical Communications (Cambridge, England). 46: 8043-5. PMID 20862423 DOI: 10.1039/C0Cc03078C |
0.793 |
|
| 2010 |
Dong Z, Plampin JN, Yap GP, Fox JM. Minimalist end groups for control of absolute helicity in salen- and salophen-based metallofoldamers. Organic Letters. 12: 4002-5. PMID 20795709 DOI: 10.1021/Ol101583V |
0.776 |
|
| 2010 |
Xie X, Yang Z, Fox JM. Stereospecific synthesis of alkylidenecyclopropanes via sequential cyclopropene carbomagnesation/1,3-carbon shift. The Journal of Organic Chemistry. 75: 3847-50. PMID 20462206 DOI: 10.1021/Jo1002938 |
0.587 |
|
| 2010 |
DeAngelis A, Boruta DT, Lubin JB, Plampin JN, Yap GP, Fox JM. The chiral crown conformation in paddlewheel complexes. Chemical Communications (Cambridge, England). 46: 4541-3. PMID 20458417 DOI: 10.1039/C001557A |
0.771 |
|
| 2010 |
Fisher LA, Zhang F, Yap GPA, Fox JM. Weak absolute helicity direction in Ni-salen by trans-cyclohexane-(1R,2R)- diamine Inorganica Chimica Acta. 364: 259-260. DOI: 10.1016/J.Ica.2010.07.044 |
0.563 |
|
| 2010 |
Fox JM, Huang X, Chieffi A, Buchwald SL. ChemInform Abstract: Highly Active and Selective Catalysts for the Formation of α-Aryl Ketones. Cheminform. 31: no-no. DOI: 10.1002/chin.200021064 |
0.426 |
|
| 2009 |
DeAngelis A, Dmitrenko O, Yap GP, Fox JM. Chiral crown conformation of Rh(2)(S-PTTL)(4): enantioselective cyclopropanation with alpha-alkyl-alpha-diazoesters. Journal of the American Chemical Society. 131: 7230-1. PMID 19469571 DOI: 10.1021/Ja9026852 |
0.799 |
|
| 2009 |
Tarwade V, Liu X, Yan N, Fox JM. Directed carbozincation reactions of cyclopropene derivatives. Journal of the American Chemical Society. 131: 5382-3. PMID 19323580 DOI: 10.1021/Ja900949N |
0.82 |
|
| 2009 |
DeAngelis A, Taylor MT, Fox JM. Unusually reactive and selective carbonyl ylides for three-component cycloaddition reactions. Journal of the American Chemical Society. 131: 1101-5. PMID 19128053 DOI: 10.1021/Ja807184R |
0.815 |
|
| 2009 |
DeAngelis A, Taylor MT, Fox JM. Three-Component Synthesis of Di- and Tetrahydrofurans underRhodium Catalysis Synfacts. 2009: 485-485. DOI: 10.1055/S-0029-1216601 |
0.351 |
|
| 2008 |
Fisher LA, Fox JM. Studies on the stability of cycloprop-2-ene carboxylate dianions and reactions with electrophiles. The Journal of Organic Chemistry. 73: 8474-8. PMID 18850746 DOI: 10.1021/Jo801683N |
0.646 |
|
| 2008 |
Tarwade V, Dmitrenko O, Bach RD, Fox JM. The Curtius rearrangement of cyclopropyl and cyclopropenoyl azides. A combined theoretical and experimental mechanistic study. The Journal of Organic Chemistry. 73: 8189-97. PMID 18826325 DOI: 10.1021/Jo801104T |
0.78 |
|
| 2008 |
Blackman ML, Royzen M, Fox JM. Tetrazine ligation: fast bioconjugation based on inverse-electron-demand Diels-Alder reactivity. Journal of the American Chemical Society. 130: 13518-9. PMID 18798613 DOI: 10.1021/Ja8053805 |
0.803 |
|
| 2008 |
Pallerla MK, Yap GP, Fox JM. Co-complexes derived from alkene insertion to alkyne-dicobaltpentacarbonyl complexes: insight into the regioselectivity of pauson-khand reactions of cyclopropenes. The Journal of Organic Chemistry. 73: 6137-41. PMID 18637694 DOI: 10.1021/Jo800776Z |
0.801 |
|
| 2008 |
Panne P, DeAngelis A, Fox JM. Rh-catalyzed intermolecular cyclopropanation with alpha-alkyl-alpha-diazoesters: catalyst-dependent chemo- and diastereoselectivity. Organic Letters. 10: 2987-9. PMID 18547051 DOI: 10.1021/Ol800983Y |
0.783 |
|
| 2008 |
Yan N, Liu X, Pallerla MK, Fox JM. Synthesis of stable derivatives of cycloprop-2-ene carboxylic acid. The Journal of Organic Chemistry. 73: 4283-6. PMID 18452335 DOI: 10.1021/Jo800042W |
0.807 |
|
| 2008 |
Royzen M, Yap GP, Fox JM. A photochemical synthesis of functionalized trans-cyclooctenes driven by metal complexation. Journal of the American Chemical Society. 130: 3760-1. PMID 18321114 DOI: 10.1021/Ja8001919 |
0.437 |
|
| 2008 |
DeAngelis A, Panne P, Yap GP, Fox JM. Rh-catalyzed formation of dioxolanes from alpha-alkyl diazoesters: diastereoselective cycloadditions of carbonyl ylides with selectivity over beta-hydride elimination. The Journal of Organic Chemistry. 73: 1435-9. PMID 18189412 DOI: 10.1021/Jo702308F |
0.786 |
|
| 2008 |
Yan N, Liu X, Fox JM. Facially selective and regioselective carbometalation of cyclopropenes by aryl Grignard reagents. The Journal of Organic Chemistry. 73: 563-8. PMID 18085796 DOI: 10.1021/Jo702176X |
0.588 |
|
| 2008 |
Pallerla MK, Fox JM. Synthesis of (-)-Pentalenene Synfacts. 2008: 449-449. DOI: 10.1055/S-2008-1072706 |
0.79 |
|
| 2008 |
Liao La, Yan N, Fox JM. Dianion approach to chiral cyclopropene carboxylic acids (Organic Letters (2004) 6) Organic Letters. 10: 3931. |
0.438 |
|
| 2007 |
Pallerla MK, Fox JM. Enantioselective synthesis of (-)-pentalenene. Organic Letters. 9: 5625-8. PMID 18031057 DOI: 10.1021/Ol702597Y |
0.806 |
|
| 2007 |
Dong Z, Yap GP, Fox JM. trans-Cyclohexane-1,2-diamine is a weak director of absolute helicity in chiral nickel-salen complexes. Journal of the American Chemical Society. 129: 11850-3. PMID 17760445 DOI: 10.1021/Ja073900P |
0.594 |
|
| 2007 |
Dong Z, Liu X, Yap GP, Fox JM. Two-dimensional scaffolds for the parallel alignment of rod-shaped conjugated molecules. The Journal of Organic Chemistry. 72: 617-25. PMID 17221982 DOI: 10.1021/Jo062261I |
0.527 |
|
| 2007 |
Panne P, Fox JM. Rh-catalyzed intermolecular reactions of alkynes with alpha-diazoesters that possess beta-hydrogens: ligand-based control over divergent pathways. Journal of the American Chemical Society. 129: 22-3. PMID 17199269 DOI: 10.1021/Ja0660195 |
0.43 |
|
| 2007 |
Fox J, Dong Z, Karpowicz Jr. R, Bai S, Yap G. Control of Helicity in a Metal Complex Synfacts. 2007: 0045-0045. DOI: 10.1055/s-2006-955675 |
0.442 |
|
| 2006 |
Dong Z, Karpowicz RJ, Bai S, Yap GP, Fox JM. Control of absolute helicity in single-stranded abiotic metallofoldamers. Journal of the American Chemical Society. 128: 14242-3. PMID 17076482 DOI: 10.1021/Ja065721Y |
0.539 |
|
| 2006 |
Zhang F, Fox JM. Synthesis of cyclopropene alpha-amino acids via enantioselective desymmetrization. Organic Letters. 8: 2965-8. PMID 16805528 DOI: 10.1021/Ol060847L |
0.386 |
|
| 2006 |
Yang Z, Xie X, Fox JM. Diastereoselective synthesis of methylenecyclopropanes from chiral cyclopropene derivatives. Angewandte Chemie (International Ed. in English). 45: 3960-2. PMID 16683292 DOI: 10.1002/Anie.200600531 |
0.578 |
|
| 2006 |
Liu X, Fox JM. Enantioselective, facially selective carbomagnesation of cyclopropenes. Journal of the American Chemical Society. 128: 5600-1. PMID 16637603 DOI: 10.1021/Ja058101Q |
0.445 |
|
| 2006 |
Fox J, Yang Z, Xie X. Diastereoselective Synthesis of Methylenecyclopropanes Synfacts. 2006: 0812-0812. DOI: 10.1055/S-2006-941949 |
0.563 |
|
| 2005 |
Pallerla MK, Fox JM. Diastereoselective intermolecular Pauson-Khand reactions of chiral cyclopropenes. Organic Letters. 7: 3593-5. PMID 16048350 DOI: 10.1021/Ol051456U |
0.814 |
|
| 2005 |
Zhang F, Bai S, Yap GP, Tarwade V, Fox JM. Abiotic metallofoldamers as electrochemically responsive molecules. Journal of the American Chemical Society. 127: 10590-9. PMID 16045347 DOI: 10.1021/Ja050886C |
0.775 |
|
| 2005 |
Fox JM, Yan N. Metal mediated and catalyzed nucleophilic additions to cyclopropenes Current Organic Chemistry. 9: 719-732. DOI: 10.2174/1385272053765006 |
0.45 |
|
| 2004 |
Liao LA, Yan N, Fox JM. Dianion approach to chiral cyclopropene carboxylic acids. Organic Letters. 6: 4937-9. PMID 15606104 DOI: 10.1021/Ol047837+ |
0.624 |
|
| 2004 |
Fox JM, Dmitrenko O, Liao LA, Bach RD. Computational studies of nucleophilic substitution at carbonyl carbon: the S(N)2 mechanism versus the tetrahedral intermediate in organic synthesis. The Journal of Organic Chemistry. 69: 7317-28. PMID 15471486 DOI: 10.1021/Jo049494Z |
0.372 |
|
| 2004 |
Liao LA, Zhang F, Dmitrenko O, Bach RD, Fox JM. A reactivity/affinity switch for parallel kinetic resolution: alpha-amino acid quasienantiomers and the resolution of cyclopropene carboxylic acids. Journal of the American Chemical Society. 126: 4490-1. PMID 15070346 DOI: 10.1021/Ja049779T |
0.356 |
|
| 2004 |
Liao LA, Zhang F, Yan N, Golen JA, Fox JM. An efficient and general method for resolving cyclopropene carboxylic acids Tetrahedron. 60: 1803-1816. DOI: 10.1016/J.Tet.2003.12.042 |
0.565 |
|
| 2004 |
Yan N, Fox JM. New methods to make monosubstituted cyclopropenes and syn-disubstituted cyclopropanes starting from acetylene Acs National Meeting Book of Abstracts. 228: ORGN-643. |
0.441 |
|
| 2002 |
Liao LA, Fox JM. A copper-catalyzed method for the facially selective addition of grignard reagents to cyclopropenes. Journal of the American Chemical Society. 124: 14322-3. PMID 12452703 DOI: 10.1021/Ja0278234 |
0.462 |
|
| 2001 |
Chieffi A, Kamikawa K, Ahman J, Fox JM, Buchwald SL. Catalytic asymmetric vinylation of ketone enolates. Organic Letters. 3: 1897-900. PMID 11405739 DOI: 10.1021/Ol0159470 |
0.787 |
|
| 2001 |
Kaye S, Fox JM, Hicks FA, Buchwald SL. The Use of Catalytic Amounts of CuCl and Other Improvements in the Benzyne Route to Biphenyl-Based Phosphine Ligands Advanced Synthesis and Catalysis. 343: 789-794. DOI: 10.1002/1615-4169(20011231)343:8<789::Aid-Adsc789>3.0.Co;2-A |
0.757 |
|
| 2000 |
Tomori H, Fox JM, Buchwald SL. An improved synthesis of functionalized biphenyl-based phosphine ligands. The Journal of Organic Chemistry. 65: 5334-41. PMID 10993363 DOI: 10.1021/Jo000691H |
0.465 |
|
| 2000 |
Fox JM, Huang X, Chieffi A, Buchwald SL. Highly active and selective catalysts for the formation of α-aryl ketones Journal of the American Chemical Society. 122: 1360-1370. DOI: 10.1021/Ja993912D |
0.652 |
|
| 1999 |
Fox JM, Katz TJ. Conversion of a [6]Helicene into an [8]Helicene and a Helical 1,10-Phenanthroline Ligand. The Journal of Organic Chemistry. 64: 302-305. PMID 11674120 DOI: 10.1021/Jo9817570 |
0.546 |
|
| 1999 |
Fox JM, Katz TJ. Conversion of a [6]helicene into an [8]helicene and a helical 1,10- phenanthroline ligand Journal of Organic Chemistry. 64: 302-305. DOI: 10.1021/jo9817570 |
0.493 |
|
| 1999 |
Fox JM, Katz TJ, Van Elshocht S, Verbiest T, Kauranen M, Persoons A, Thongpanchang T, Krauss T, Brus L. Synthesis, self-assembly, and nonlinear optical properties of conjugated helical metal phthalocyanine derivatives Journal of the American Chemical Society. 121: 3453-3459. DOI: 10.1021/Ja983633A |
0.517 |
|
| 1998 |
Fox JM, Goldberg NR, Katz TJ. Efficient Synthesis of Functionalized [7]Helicenes. The Journal of Organic Chemistry. 63: 7456-7462. PMID 11672398 DOI: 10.1021/Jo981380Y |
0.614 |
|
| 1998 |
Fox JM, Lin D, Itagaki Y, Fujita T. Synthesis of Conjugated Helical Acetylene-Bridged Polymers and Cyclophanes Journal of Organic Chemistry. 63: 2031-2038. DOI: 10.1021/Jo972101U |
0.305 |
|
| 1997 |
Katz TJ, Liu L, Willmore ND, Fox JM, Rheingold AL, Shi S, Nuckolls C, Rickman BH. An efficient synthesis of functionalized helicenes Journal of the American Chemical Society. 119: 10054-10063. DOI: 10.1021/Ja9721327 |
0.681 |
|
| 1992 |
Fox JM, Gillen Scacheri JE, Jones KL, Jones M, B. Shevlin P, Armstrong B, Sztyrbicka R. The phenylcarbene rearrangement as a source of real carbenes. Tetrahedron Letters. 33: 5021-5024. DOI: 10.1016/S0040-4039(00)61178-4 |
0.314 |
|
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