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Travis J. Williams, Ph.D. - Publications

Affiliations: 
Chemistry University of Southern California, Los Angeles, CA, United States 
Area:
Organometallic Chemistry
Website:
http://chem.usc.edu/faculty/Williams.html
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90 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Zhang L, Lu Z, Rander AR, Williams TJ. An ambient pressure, direct hydrogenation of ketones. Chemical Communications (Cambridge, England). 59: 8107-8110. PMID 37294535 DOI: 10.1039/d3cc01014g  0.543
2023 Nalikezhathu A, Tam A, Cherepakhin V, Do VK, Williams TJ. Synthesis of 1,4-Diazacycles by Hydrogen Borrowing. Organic Letters. PMID 36867725 DOI: 10.1021/acs.orglett.3c00468  0.381
2022 Do VK, Vargas NA, Chavez AJ, Zhang L, Cherepakhin V, Lu Z, Currier RP, Dub PA, Gordon JC, Williams TJ. Pressurized Formic Acid Dehydrogenation: An Entropic Spring Replaces Hydrogen Compression Cost. Catalysis Science & Technology. 12: 7182-7189. PMID 37192930 DOI: 10.1039/d2cy00676f  0.542
2020 Cherepakhin V, Hellman A, Lan Z, Mallikarjun Sharada S, Williams TJ. Heterobimetallic complexes of IrM (M = Fe, Co, and Ni) core and bridging 2-(diphenylphosphino)pyridine: electronic structure and electrochemical behavior. Dalton Transactions (Cambridge, England : 2003). 49: 10509-10515. PMID 32748911 DOI: 10.1039/D0Dt01801E  0.357
2020 Nalikezhathu A, Cherepakhin V, Williams TJ. Ruthenium Catalyzed Tandem Pictet-Spengler Reaction. Organic Letters. PMID 32558575 DOI: 10.1021/Acs.Orglett.0C01485  0.356
2020 Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508  0.303
2020 Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508  0.303
2020 Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508  0.303
2020 Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508  0.303
2020 Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508  0.303
2020 Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508  0.303
2020 Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508  0.303
2020 Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508  0.303
2020 Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508  0.303
2020 Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508  0.303
2020 Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508  0.303
2020 Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508  0.303
2020 Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508  0.303
2020 Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508  0.303
2020 Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508  0.303
2020 Demianets I, Cherepakhin V, Maertens A, Lauridsen PJ, Sharada SM, Williams TJ. A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron. 182. PMID 32410767 DOI: 10.1016/J.Poly.2020.114508  0.303
2019 Cherepakhin V, Williams TJ. Catalyst Evolution in Ruthenium-Catalyzed Coupling of Amines and Alcohols Acs Catalysis. 10: 56-65. DOI: 10.1021/Acscatal.9B03679  0.369
2019 Demianets I, Hunt JR, Dawlaty JM, Williams TJ. Optical pKa Control in a Bifunctional Iridium Complex Organometallics. 38: 200-204. DOI: 10.1021/Acs.Organomet.8B00778  0.429
2018 Lu Z, Cherepakhin V, Kapenstein T, Williams TJ. Upgrading Biodiesel from Vegetable Oils by Hydrogen Transfer to its Fatty Esters. Acs Sustainable Chemistry & Engineering. 6: 5749-5753. PMID 30319930 DOI: 10.1021/Acssuschemeng.8B00653  0.589
2018 Cherepakhin V, Williams TJ. Iridium Catalysts for Acceptorless Dehydrogenation of Alcohols to Carboxylic Acids: Scope and Mechanism. Acs Catalysis. 8: 3754-3763. PMID 30288338 DOI: 10.1021/Acscatal.8B00105  0.409
2018 Navarro CA, Kedzie EA, Ma Y, Michael KH, Nutt SR, Williams TJ. Mechanism and Catalysis of Oxidative Degradation of Fiber-Reinforced Epoxy Composites. Topics in Catalysis. 61: 704-709. PMID 30288016 DOI: 10.1007/S11244-018-0917-2  0.31
2018 Lauridsen PJ, Lu Z, Celaje JJA, Kedzie EA, Williams TJ. Conformational twisting of a formate-bridged diiridium complex enables catalytic formic acid dehydrogenation. Dalton Transactions (Cambridge, England : 2003). PMID 30206593 DOI: 10.1039/C8Dt03268H  0.784
2018 Lu Z, Cherepakhin V, Demianets I, Lauridsen PJ, Williams TJ. Iridium-based hydride transfer catalysts: from hydrogen storage to fine chemicals. Chemical Communications (Cambridge, England). PMID 29888372 DOI: 10.1039/C8Cc03412E  0.622
2017 Lee H, Feakins SJ, Lu Z, Schimmelmann A, Sessions AL, Tierney JE, Williams TJ. Comparison of three methods for the methylation of aliphatic and aromatic compounds. Rapid Communications in Mass Spectrometry : Rcm. PMID 28763166 DOI: 10.1002/Rcm.7947  0.527
2017 Celaje JJA, Zhang X, Zhang F, Kam L, Herron JR, Williams TJ. A Base and Solvent-Free Ruthenium-Catalyzed Alkylation of Amines Acs Catalysis. 7: 1136-1142. DOI: 10.1021/Acscatal.6B03088  0.836
2016 Zhang X, Kam L, Trerise R, Williams TJ. Ruthenium-Catalyzed Ammonia Borane Dehydrogenation: Mechanism and Utility. Accounts of Chemical Research. PMID 28032510 DOI: 10.1021/Acs.Accounts.6B00482  0.455
2016 Celaje JJ, Lu Z, Kedzie EA, Terrile NJ, Lo JN, Williams TJ. A prolific catalyst for dehydrogenation of neat formic acid. Nature Communications. 7: 11308. PMID 27076111 DOI: 10.1038/Ncomms11308  0.8
2016 Zhang X, Kam L, Williams TJ. Dehydrogenation of ammonia borane through the third equivalent of hydrogen. Dalton Transactions (Cambridge, England : 2003). PMID 27052687 DOI: 10.1039/C6Dt00604C  0.346
2016 Lu Z, Williams TJ. Di(carbene)-Supported Nickel Systems for CO2 Reduction under Ambient Conditions Acs Catalysis. 6: 6670-6673. DOI: 10.1021/Acscatal.6B02101  0.634
2016 Lu Z, Demianets I, Hamze R, Terrile NJ, Williams TJ. A Prolific Catalyst for Selective Conversion of Neat Glycerol to Lactic Acid Acs Catalysis. 6: 2014-2017. DOI: 10.1021/Acscatal.5B02732  0.621
2015 Zhang X, Lu Z, Foellmer LK, Williams TJ. Nitrogen-Based Ligands Accelerate Ammonia Borane Dehydrogenation with the Shvo Catalyst Organometallics. 34: 3732-3738. DOI: 10.1021/Acs.Organomet.5B00409  0.655
2014 Pennington-Boggio MK, Conley BL, Richmond MG, Williams TJ. Synthesis, Structure, and Conformational Dynamics of Rhodium and Iridium Complexes of Dimethylbis(2-pyridyl)borate. Polyhedron. 84: 24-31. PMID 25435645 DOI: 10.1016/J.Poly.2014.05.042  0.773
2014 Wu X, Dawsey AC, Siriwardena-Mahanama BN, Allen MJ, Williams TJ. A (Fluoroalkyl)Guanidine Modulates the Relaxivity of a Phosphonate-Containing T 1-Shortening Contrast Agent. Journal of Fluorine Chemistry. 168: 177-183. PMID 25431503 DOI: 10.1016/J.Jfluchem.2014.09.018  0.756
2014 Celaje JA, Pennington-Boggio MK, Flaig RW, Richmond MG, Williams TJ. Synthesis and Characterization of Dimethylbis(2-pyridyl)borate Nickel(II) Complexes: Unimolecular Square-Planar to Square-Planar Rotation around Nickel(II). Organometallics. 33: 2019-2026. PMID 24882919 DOI: 10.1021/Om500173J  0.754
2014 Krylova VA, Djurovich PI, Conley BL, Haiges R, Whited MT, Williams TJ, Thompson ME. Control of emission colour with N-heterocyclic carbene (NHC) ligands in phosphorescent three-coordinate Cu(I) complexes. Chemical Communications (Cambridge, England). 50: 7176-9. PMID 24853355 DOI: 10.1039/C4Cc02037E  0.742
2014 Lu Z, Williams TJ. A dual site catalyst for mild, selective nitrile reduction. Chemical Communications (Cambridge, England). 50: 5391-3. PMID 24409456 DOI: 10.1039/C3Cc47384H  0.653
2014 Li V, Ghang YJ, Hooley RJ, Williams TJ. Non-covalent self assembly controls the relaxivity of magnetically active guests. Chemical Communications (Cambridge, England). 50: 1375-7. PMID 24346341 DOI: 10.1039/C3Cc48389D  0.493
2013 Dawsey AC, Hathaway KL, Kim S, Williams TJ. Introductory Chemistry: A Molar Relaxivity Experiment in the High School Classroom. Journal of Chemical Education. 90: 922-925. PMID 23929983 DOI: 10.1021/Ed3006902  0.759
2013 Li V, Chang AY, Williams TJ. A noncovalent, fluoroalkyl coating monomer for phosphonate-covered nanoparticles. Tetrahedron. 69: 7741-7746. PMID 23913989 DOI: 10.1016/J.Tet.2013.05.092  0.482
2012 Lu Z, Conley BL, Williams TJ. A Three-Stage Mechanistic Model for Ammonia Borane Dehydrogenation by Shvo's Catalyst. Organometallics. 31: 6705-6714. PMID 23335832 DOI: 10.1021/Om300562D  0.818
2012 Pennington-Boggio MK, Conley BL, Williams TJ. A Ruthenium-Catalyzed Coupling of Alkynes with 1,3-Diketones. Journal of Organometallic Chemistry. 716: 6-10. PMID 22923850 DOI: 10.1016/J.Jorganchem.2012.05.017  0.815
2012 Dawsey AC, Li V, Hamilton KC, Wang J, Williams TJ. Copper-catalyzed oxidation of azolines to azoles. Dalton Transactions (Cambridge, England : 2003). 41: 7994-8002. PMID 22460353 DOI: 10.1039/C2Dt00025C  0.8
2012 Lu Z, Malinoski B, Flores AV, Conley BL, Guess D, Williams TJ. Alcohol dehydrogenation with a dual site ruthenium, Boron Catalyst occurs at ruthenium Catalysts. 2: 412-421. DOI: 10.3390/Catal2040412  0.786
2012 Wu X, Boz E, Sirkis AM, Chang AY, Williams TJ. Synthesis and phosphonate binding of guanidine-functionalized fluorinated amphiphiles Journal of Fluorine Chemistry. 135: 292-302. DOI: 10.1016/J.Jfluchem.2011.12.011  0.66
2011 Conley BL, Guess D, Williams TJ. A robust, air-stable, reusable ruthenium catalyst for dehydrogenation of ammonia borane. Journal of the American Chemical Society. 133: 14212-5. PMID 21827173 DOI: 10.1021/Ja2058154  0.758
2011 Williams TJ, Kershaw AD, Li V, Wu X. An Inversion Recovery NMR Kinetics Experiment. Journal of Chemical Education. 88: 665-669. PMID 21552343 DOI: 10.1021/Ed1006822  0.703
2011 Conley BL, Williams TJ. Dual site catalysts for hydride manipulation Comments On Inorganic Chemistry. 32: 195-218. DOI: 10.1080/02603594.2011.642087  0.776
2010 Conley BL, Williams TJ. Dehydrogenation of ammonia-borane by Shvo's catalyst. Chemical Communications (Cambridge, England). 46: 4815-7. PMID 20508879 DOI: 10.1039/C003157G  0.76
2010 Wender PA, Sirois LE, Stemmler RT, Williams TJ. Highly efficient, facile, room temperature intermolecular [5 + 2] cycloadditions catalyzed by cationic rhodium(I): one step to cycloheptenes and their libraries. Organic Letters. 12: 1604-7. PMID 20196579 DOI: 10.1021/Ol100337M  0.571
2010 Conley BL, Pennington-Boggio MK, Boz E, Williams TJ. Discovery, applications, and catalytic mechanisms of Shvo's catalyst. Chemical Reviews. 110: 2294-312. PMID 20095576 DOI: 10.1021/Cr9003133  0.784
2010 Conley BL, Williams TJ. Thermochemistry and molecular structure of a remarkable agostic interaction in a heterobifunctional ruthenium-boron complex. Journal of the American Chemical Society. 132: 1764-5. PMID 20088526 DOI: 10.1021/Ja909858A  0.737
2010 Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. ChemInform Abstract: Toward the Ideal Synthesis: New Transition Metal catalyzed Reactions Inspired by Novel Medicinal Leads Cheminform. 33: no-no. DOI: 10.1002/chin.200241295  0.835
2010 Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. ChemInform Abstract: Toward the Ideal Synthesis: New Transition Metal catalyzed Reactions Inspired by Novel Medicinal Leads Cheminform. 33: no-no. DOI: 10.1002/chin.200241295  0.835
2010 Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. ChemInform Abstract: Toward the Ideal Synthesis: New Transition Metal catalyzed Reactions Inspired by Novel Medicinal Leads Cheminform. 33: no-no. DOI: 10.1002/chin.200241295  0.835
2010 Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. ChemInform Abstract: Toward the Ideal Synthesis: New Transition Metal catalyzed Reactions Inspired by Novel Medicinal Leads Cheminform. 33: no-no. DOI: 10.1002/chin.200241295  0.835
2009 Thorson MK, Klinkel KL, Wang J, Williams TJ. Mechanism of hydride abstraction by cyclopentadienone-ligated carbonylmetal complexes (M = Ru, Fe) European Journal of Inorganic Chemistry. 295-302. DOI: 10.1002/Ejic.200800975  0.433
2008 Williams TJ, Caffyn AJ, Hazari N, Oblad PF, Labinger JA, Bercaw JE. C-H bond activation by air-stable [(diimine)M(II)(mu2-OH)]2(2+) dimers (M = Pd, Pt). Journal of the American Chemical Society. 130: 2418-9. PMID 18237167 DOI: 10.1021/Ja076740Q  0.79
2008 Bercaw JE, Hazari N, Williams TJ, Caffyn AJM, Oblad PF, Labinger JA. Carbon-hydrogen bond activation with platinum and palladium complexes Acs National Meeting Book of Abstracts.  0.765
2007 Williams TJ, Labinger JA, Bercaw JE. Reactions of Indene and Indoles with Platinum Methyl Cations: Indene C-H Activation, Indole π vs. Nitrogen Lone-Pair Coordination. Organometallics. 26: 281-287. PMID 27087735 DOI: 10.1021/Om0606643  0.495
2007 Driver TG, Williams TJ, Labinger JA, Bercaw JE. C-H bond activation by dicationic platinum(II) complexes Organometallics. 26: 294-301. DOI: 10.1021/Om060792R  0.697
2007 Williams TJ, Labinger JA, Bercaw JE. Reactions of indene and indoles with platinum methyl cations: Indene C-H activation, indole π versus nitrogen lone-pair coordination Organometallics. 26: 281-287. DOI: 10.1021/om0606643  0.495
2006 Wender PA, Paxton TJ, Williams TJ. Cyclopentadienone synthesis by rhodium(I)-catalyzed [3 + 2] cycloaddition reactions of cyclopropenones and alkynes. Journal of the American Chemical Society. 128: 14814-5. PMID 17105285 DOI: 10.1021/Ja065868P  0.627
2006 Wender PA, Haustedt LO, Lim J, Love JA, Williams TJ, Yoon JY. Asymmetric catalysis of the [5 + 2] cycloaddition reaction of vinylcyclopropanes and pi-systems. Journal of the American Chemical Society. 128: 6302-3. PMID 16683779 DOI: 10.1021/Ja058590U  0.741
2006 Wender P, Haustedt L, Lim J, Love J, Williams T, Yoon J. Asymmetric [5+2] Cycloaddition of Vinylcyclopropanes and π-Systems Synfacts. 2006: 0809-0809. DOI: 10.1055/S-2006-942016  0.605
2006 Wender P, Haustedt L, Lim J, Love J, Williams T, Yoon J. Asymmetric [5+2] Cycloaddition of Vinylcyclopropanes and π-Systems Synfacts. 2006: 0809-0809. DOI: 10.1055/S-2006-942016  0.605
2006 Wender P, Haustedt L, Lim J, Love J, Williams T, Yoon J. Asymmetric [5+2] Cycloaddition of Vinylcyclopropanes and π-Systems Synfacts. 2006: 0809-0809. DOI: 10.1055/S-2006-942016  0.605
2006 Wender P, Haustedt L, Lim J, Love J, Williams T, Yoon J. Asymmetric [5+2] Cycloaddition of Vinylcyclopropanes and π-Systems Synfacts. 2006: 0809-0809. DOI: 10.1055/S-2006-942016  0.605
2005 Wender PA, Gamber GG, Williams TJ. Rhodium(I)-Catalyzed [5+2], [6+2], and [5+2+1] Cycloadditions: New Reactions for Organic Synthesis Modern Rhodium-Catalyzed Organic Reactions. 263-299. DOI: 10.1002/3527604693.ch13  0.823
2004 Wender PA, Deschamps NM, Williams TJ. Intermolecular dienyl Pauson-Khand reaction. Angewandte Chemie (International Ed. in English). 43: 3076-9. PMID 15188486 DOI: 10.1002/Anie.200454117  0.809
2003 Wender PA, Baryza JL, Brenner SE, Clarke MO, Gamber GG, Horan JC, Jessop TC, Kan C, Pattabiraman K, Williams TJ. Inspirations from nature. New reactions, new therapeutic leads, and new drug delivery systems Pure and Applied Chemistry. 75: 143-155. DOI: 10.1351/Pac200375020143  0.772
2003 Wender PA, Love JA, Williams TJ. Rhodium-catalyzed [5+2] cycloaddition reactions in water Synlett. 1295-1298. DOI: 10.1055/S-2003-40357  0.716
2003 Wender PA, Baryza JL, Brenner SE, Clarke MO, Gamber GG, Horan JC, Jessop TC, Kan C, Pattabiraman K, Williams TJ. Inspirations from nature. New reactions, therapeutic leads, and drug delivery systems Pure and Applied Chemistry. 75: 143-155.  0.755
2002 Wender PA, Williams TJ. [(arene)Rh(cod)]+ Complexes as catalysts for [5+2] cycloaddition reactions. Angewandte Chemie (International Ed. in English). 41: 4550-3. PMID 12458535 DOI: 10.1002/1521-3773(20021202)41:23<4550::Aid-Anie4550>3.0.Co;2-D  0.634
2002 Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025  0.857
2002 Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025  0.857
2002 Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025  0.857
2002 Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025  0.857
2002 Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025  0.857
2002 Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025  0.857
2002 Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025  0.857
2002 Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025  0.857
2002 Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025  0.857
2002 Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025  0.857
2002 Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/pac200274010025  0.857
2002 Wender PA, Bi FC, Gamber GG, Gosselin F, Hubbard RD, Scanio MJC, Sun R, Williams TJ, Zhang L. Toward the ideal synthesis. New transition metal-catalyzed reactions inspired by novel medicinal leads Pure and Applied Chemistry. 74: 25-31. DOI: 10.1351/Pac200274010025  0.851
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