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Jeffrey B. Johnson, Ph.D. - Publications

Affiliations: 
2000-2004 Chemistry University of Wisconsin, Madison, Madison, WI 
 2005-2007 Chemistry Colorado State University, Fort Collins, CO 
 2007- Chemistry Hope College, Holland, MI, United States 
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16 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
2017 Gregerson CE, Trentadue KN, Phipps EJT, Kirsch JK, Reed KM, Dyke GD, Jansen JH, Otteman CB, Stachowski JL, Johnson JB. Oxidative coupling of Michael acceptors with aryl nucleophiles produced through rhodium-catalyzed C-C bond activation. Organic & Biomolecular Chemistry. PMID 28675229 DOI: 10.1039/c7ob01212h  0.351
2016 Dennis JM, Compagner CT, Dorn SK, Johnson JB. Rhodium-Catalyzed Interconversion of Quinolinyl Ketones with Boronic Acids via C-C Bond Activation. Organic Letters. PMID 27367643 DOI: 10.1021/acs.orglett.6b01434  0.311
2012 Lutz JP, Rathbun CM, Stevenson SM, Powell BM, Boman TS, Baxter CE, Zona JM, Johnson JB. Rate-limiting step of the Rh-catalyzed carboacylation of alkenes: C-C bond activation or migratory insertion? Journal of the American Chemical Society. 134: 715-22. PMID 22133417 DOI: 10.1021/ja210307s  0.364
2010 Casey CP, Johnson JB, Jiao X, Beetner SE, Singer SW. Chain mechanism for exchange of D2 with a ruthenium hydride. Chemical Communications (Cambridge, England). 46: 7915-7. PMID 20856982 DOI: 10.1039/C0Cc02875D  0.655
2008 Williams CM, Johnson JB, Rovis T. Nickel-catalyzed reductive carboxylation of styrenes using CO2. Journal of the American Chemical Society. 130: 14936-7. PMID 18928253 DOI: 10.1021/Ja8062925  0.31
2008 Johnson JB, Rovis T. Enantioselective cross-coupling of anhydrides with organozinc reagents: the controlled formation of carbon-carbon bonds through the nucleophilic interception of metalacycles. Accounts of Chemical Research. 41: 327-38. PMID 18232665 DOI: 10.1021/Ar700176T  0.326
2008 Casey CP, Beetner SE, Johnson JB. 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. Journal of the American Chemical Society. 130: 2285-95. PMID 18215043 DOI: 10.1021/Ja077525C  0.737
2008 Casey CP, Johnson JB, Singer SW, Cui Q. Hydrogen elimination from a hydroxycyclopentadienyl ruthenium(II) hydride: Study of hydrogen activation in a ligand-metal bifunctional hydrogenation catalyst (Journal of the American Chemical Society (2005) 127, (3100-3109)) Journal of the American Chemical Society. 130: 1110. DOI: 10.1021/Ja710851Z  0.733
2007 Johnson JB, Bercot EA, Rowley JM, Coates GW, Rovis T. Ligand-dependent catalytic cycle and role of styrene in nickel-catalyzed anhydride cross-coupling: evidence for turnover-limiting reductive elimination. Journal of the American Chemical Society. 129: 2718-25. PMID 17295486 DOI: 10.1021/Ja067845G  0.337
2006 Casey CP, Strotman NA, Beetner SE, Johnson JB, Priebe DC, Guzei IA. PPh 3-Substituted[2,5-Ph 2-3,4-Tol 2(η 5-C 4COH)]Ru(CO)(PPh 3)H exhibits slower stoichiometric reduction, faster catalytic hydrogenation, and higher chemoselectivity for hydrogenation of aldehydes over ketones than the dicarbonyl Shvo catalyst Organometallics. 25: 1236-1244. DOI: 10.1021/Om050939Z  0.723
2006 Casey CP, Strotman NA, Beetner SE, Johnson JB, Priebe DC, Vos TE, Khodavandi B, Guzei IA. The PPh 3-substituted hydroxycyclopentadienyl ruthenium hydride [2,5-Ph 2-3,4-Tol 2(η 5-C 4COH)] Ru(CO)(PPh 3)H is a more efficient catalyst for hydrogenation of aldehydes Organometallics. 25: 1230-1235. DOI: 10.1021/Om0509387  0.627
2005 Casey CP, Johnson JB, Singer SW, Cui Q. Hydrogen elimination from a hydroxycyclopentadienyl ruthenium(II) hydride: study of hydrogen activation in a ligand-metal bifunctional hydrogenation catalyst. Journal of the American Chemical Society. 127: 3100-9. PMID 15740149 DOI: 10.1021/Ja043460R  0.761
2005 Casey CP, Johnson JB. Isomerization and deuterium scrambling evidence for a change in the rate-limiting step during imine hydrogenation by Shvo's hydroxycyclopentadienyl ruthenium hydride. Journal of the American Chemical Society. 127: 1883-94. PMID 15701023 DOI: 10.1021/Ja044450T  0.528
2005 Casey CP, Johnson JB. 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 Canadian Journal of Chemistry. 83: 1339-1346. DOI: 10.1139/V05-140  0.606
2003 Johnson JB, Bäckvall JE. Mechanism of ruthenium-catalyzed hydrogen transfer reactions. Concerted transfer of OH and CH hydrogens from an alcohol to a (Cyclopentadienone)ruthenium complex. The Journal of Organic Chemistry. 68: 7681-4. PMID 14510542 DOI: 10.1021/jo034634a  0.365
2003 Casey CP, Johnson JB. Kinetic isotope effect evidence for a concerted hydrogen transfer mechanism in transfer hydrogenations catalyzed by [p-(Me2CH)C6H4Me]Ru- (NHCHPhCHPhNSO2C6H4-p-CH3). The Journal of Organic Chemistry. 68: 1998-2001. PMID 12608822 DOI: 10.1021/Jo0205457  0.551
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