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 |
|
Show low-probability matches. |