Jeffrey B. Johnson

发表

THE STERIC COURSES OF CHEMICAL REACTIONS. 3. COMPUTER GENERATION OF PRODUCT DISTRIBUTIONS, STERIC COURSES, AND PERMUTATIONAL ISOMERS

M. G. Hutchings, W. G. Klemperer, Jeffrey B. Johnson, 1978 .

Ligand differentiated complementary Rh-catalyst systems for the enantioselective desymmetrization of meso-cyclic anhydrides

J. B. Johnson, T. Rovis, M. Cook, 2009 .

A concise synthesis of eupomatilones 4, 6, and 7 by rhodium-catalyzed enantioselective desymmetrization of cyclic meso anhydrides with organozinc reagents generated in situ.

C. M. Williams, J. B. Johnson, T. Rovis, 2007, Angewandte Chemie.

Enantioselective cross-coupling of anhydrides with organozinc reagents: the controlled formation of carbon-carbon bonds through the nucleophilic interception of metalacycles.

J. B. Johnson, T. Rovis, Jeffrey B. Johnson, 2008, Accounts of chemical research.

Kinetic isotope effect evidence for the concerted transfer of hydride and proton from hydroxycyclopentadienyl ruthenium hydride in solvents of different polarities and hydrogen bonding ability

J. B. Johnson, Jeffrey B. Johnson, C. Casey, 2005 .

Mechanism of ruthenium-catalyzed hydrogen transfer reactions. Evidence for a stepwise transfer of CH and NH hydrogens from an amine to a (cyclopentadienone)ruthenium complex

J. Bäckvall, J. B. Johnson, Jeffrey B. Johnson, 2003 .

A molecular orbital analysis of electronic structure and bonding in chromium hexacarbonyl

W. Klemperer, J. B. Johnson, Jeffrey B. Johnson, 1977 .

More than bystanders: the effect of olefins on transition-metal-catalyzed cross-coupling reactions.

J. B. Johnson, T. Rovis, Jeffrey B. Johnson, 2008, Angewandte Chemie.

Selective substituent transfer from mixed zinc reagents in Ni-catalyzed anhydride alkylation.

J. B. Johnson, T. Rovis, Jeffrey B. Johnson, 2006, Organic letters.

Steric and electronic effects influencing β-aryl elimination in the Pd-catalyzed carbon-carbon single bond activation of triarylmethanols.

Valerie J. Winton, J. B. Johnson, James R Bour, 2013, The Journal of organic chemistry.

Rate-limiting step of the Rh-catalyzed carboacylation of alkenes: C-C bond activation or migratory insertion?

Colin M. Rathbun, J. Lutz, J. B. Johnson, 2012, Journal of the American Chemical Society.

Rhodium-catalyzed acylation with quinolinyl ketones: carbon-carbon single bond activation as the turnover-limiting step of catalysis.

Colin M. Rathbun, J. B. Johnson, Jeffrey B. Johnson, 2011, Journal of the American Chemical Society.

Hydrogen elimination from a hydroxycyclopentadienyl ruthenium(II) hydride: study of hydrogen activation in a ligand-metal bifunctional hydrogenation catalyst.

Q. Cui, S. Singer, J. B. Johnson, 2005, Journal of the American Chemical Society.

Ring Opening of Epoxides, Aziridines and Cyclic Anhydrides

Jeffrey B. Johnson, 2011 .

Kinetic isotope effect evidence for a concerted hydrogen transfer mechanism in transfer hydrogenations catalyzed by [p-(Me2CH)C6H4Me]Ru- (NHCHPhCHPhNSO2C6H4-p-CH3).

J. B. Johnson, Jeffrey B. Johnson, C. Casey, 2003, The Journal of organic chemistry.

Nickel-catalyzed reductive carboxylation of styrenes using CO2.

C. M. Williams, J. B. Johnson, T. Rovis, 2008, Journal of the American Chemical Society.

Mechanism of ruthenium-catalyzed hydrogen transfer reactions. Concerted transfer of OH and CH hydrogens from an alcohol to a (Cyclopentadienone)ruthenium complex.

J. Bäckvall, J. B. Johnson, Jeffrey B. Johnson, 2003, The Journal of organic chemistry.

Pyridine-directed carbon–carbon single bond activation: Rhodium-catalyzed decarbonylation of aryl and heteroaromatic ketones

Cole J. Wagner, Eric A. Salisbury, Erik J. Schoonover, 2021 .

Nickel-mediated decarbonylative cross-coupling of phthalimides with in situ generated diorganozinc reagents.

Valerie J. Winton, J. B. Johnson, Jeffrey B. Johnson, 2011, The Journal of organic chemistry.

Ligand-dependent catalytic cycle and role of styrene in nickel-catalyzed anhydride cross-coupling: evidence for turnover-limiting reductive elimination.

G. Coates, T. Rovis, J. Rowley, 2007, Journal of the American Chemical Society.

Nickel‐Catalyzed Reductive Carboxylation of Styrenes Using CO2.

C. M. Williams, T. Rovis, Jeffrey B. Johnson, 2009 .

Isomerization and deuterium scrambling evidence for a change in the rate-limiting step during imine hydrogenation by Shvo's hydroxycyclopentadienyl ruthenium hydride.

J. B. Johnson, Jeffrey B. Johnson, C. Casey, 2005, Journal of the American Chemical Society.

PPh3-Substituted [2,5-Ph2-3,4-Tol2(η5-C4COH)]Ru(CO)(PPh3)H Exhibits Slower Stoichiometric Reduction, Faster Catalytic Hydrogenation, and Higher Chemoselectivity for Hydrogenation of Aldehydes over Ketones Than the Dicarbonyl Shvo Catalyst

I. Guzei, Jeffrey B. Johnson, C. Casey, 2006 .

Decarbonylative cross coupling of phthalimides with diorganozinc reagents—Efforts toward catalysis

J. B. Johnson, Kimberly Deglopper, Jeffrey B. Johnson, 2016 .

Rate-limiting step of the Rh-catalyzed carboacylation of alkenes: C-C bond activation or migratory insertion?

Colin M. Rathbun, J. Lutz, Jeffrey B. Johnson, 2012, Journal of the American Chemical Society.

Rhodium-catalyzed acylation with quinolinyl ketones: carbon-carbon single bond activation as the turnover-limiting step of catalysis.

Colin M. Rathbun, Jeffrey B. Johnson, 2011, Journal of the American Chemical Society.

Oxidative coupling of Michael acceptors with aryl nucleophiles produced through rhodium-catalyzed C-C bond activation.

J. B. Johnson, Caroline Gregerson, Kathryn Trentadue, 2017, Organic & biomolecular chemistry.

Rhodium-Catalyzed Interconversion of Quinolinyl Ketones with Boronic Acids via C-C Bond Activation.

J. Dennis, Chad T. Compagner, S. Dorn, 2016, Organic Letters.

Spectroscopic determination of hydrogenation rates and intermediates during carbonyl hydrogenation catalyzed by Shvo's hydroxycyclopentadienyl diruthenium hydride agrees with kinetic modeling based on independently measured rates of elementary reactions.

J. B. Johnson, Jeffrey B. Johnson, C. Casey, 2008, Journal of the American Chemical Society.