Year |
Citation |
Score |
2012 |
Keith JA, Behenna DC, Sherden N, Mohr JT, Ma S, Marinescu SC, Nielsen RJ, Oxgaard J, Stoltz BM, Goddard WA. The reaction mechanism of the enantioselective Tsuji allylation: inner-sphere and outer-sphere pathways, internal rearrangements, and asymmetric C-C bond formation. Journal of the American Chemical Society. 134: 19050-60. PMID 23102088 DOI: 10.1021/Ja306860N |
0.394 |
|
2008 |
Jacobsson M, Oxgaard J, Abrahamsson CO, Norrby PO, Goddard WA, Ellervik U. Acid-catalyzed nucleophilic aromatic substitution: experimental and theoretical exploration of a multistep mechanism. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 3954-60. PMID 18351696 DOI: 10.1002/Chem.200701590 |
0.433 |
|
2007 |
Gonzales JM, Distasio R, Periana RA, Goddard WA, Oxgaard J. Methylrhenium trioxide revisited: mechanisms for nonredox oxygen insertion in an M-CH3 bond. Journal of the American Chemical Society. 129: 15794-804. PMID 18052160 DOI: 10.1021/Ja0714742 |
0.325 |
|
2007 |
Keith JA, Nielsen RJ, Oxgaard J, Goddard WA. Unraveling the Wacker oxidation mechanisms. Journal of the American Chemical Society. 129: 12342-3. PMID 17880213 DOI: 10.1021/Ja072400T |
0.351 |
|
2007 |
Keith JA, Behenna DC, Mohr JT, Ma S, Marinescu SC, Oxgaard J, Stoltz BM, Goddard WA. The inner-sphere process in the enantioselective Tsuji allylation reaction with (S)-t-Bu-phosphinooxazoline ligands. Journal of the American Chemical Society. 129: 11876-7. PMID 17824701 DOI: 10.1021/Ja070516J |
0.369 |
|
2006 |
Keith JM, Muller RP, Kemp RA, Goldberg KI, Goddard WA, Oxgaard J. Mechanism of direct molecular oxygen insertion in a palladium(II)-hydride bond. Inorganic Chemistry. 45: 9631-3. PMID 17112254 DOI: 10.1021/Ic061392Z |
0.352 |
|
2005 |
Bhalla G, Oxgaard J, Goddard WA, Periana RA. Hydrovinylation of olefins catalyzed by an iridium complex via CH activation Organometallics. 24: 5499-5502. DOI: 10.1021/Om050614I |
0.348 |
|
2004 |
Oxgaard J, Muller RP, Goddard WA, Periana RA. Mechanism of homogeneous Ir(III) catalyzed regioselective arylation of olefins. Journal of the American Chemical Society. 126: 352-63. PMID 14709102 DOI: 10.1021/Ja034126I |
0.338 |
|
2003 |
Wiest O, Oxgaard J, Saettel NJ. Structure and reactivity of hydrocarbon radical cations Advances in Physical Organic Chemistry. 38: 87-109. DOI: 10.1016/S0065-3160(03)38002-5 |
0.672 |
|
2003 |
Oxgaard J, Wiest O. Substituent Effects in the Vinylcyclopropane Radical Cation Rearrangement: A Computational Road to a New Synthetic Tool European Journal of Organic Chemistry. 2003: 1454-1462. DOI: 10.1002/Ejoc.200390204 |
0.668 |
|
2003 |
Oxgaard J, Wiest O. Substituent effects in the vinylcyclopropane radical cation rearrangement: A computational road to a new synthetic tool European Journal of Organic Chemistry. 1454-1462. |
0.451 |
|
2002 |
Oxgaard J, Wiest O. Rehybridized 1,3-butadiene radical cations: How far will a radical cation go to maintain conjugation? Journal of Physical Chemistry A. 106: 3967-3974. DOI: 10.1021/Jp020041C |
0.657 |
|
2001 |
Oxgaard J, Wiest O. Symmetry, radical ions, and butadienes: Exploring the limits of density functional theory Journal of Physical Chemistry A. 105: 8236-8240. DOI: 10.1021/Jp011336D |
0.638 |
|
2001 |
Saettel NJ, Oxgaard J, Wiest O. Pericyclic Reactions of Radical Cations European Journal of Organic Chemistry. 2001: 1429-1439. DOI: 10.1002/1099-0690(200104)2001:8<1429::Aid-Ejoc1429>3.0.Co;2-6 |
0.695 |
|
2001 |
Saettel NJ, Oxgaard J, Wiest O. Pericyclic reactions of radical cations European Journal of Organic Chemistry. 1429-1439. |
0.691 |
|
1999 |
Oxgaard J, Wiest O. The vinylcyclopropane radical cation rearrangement and related: Reactions on the C5H8·+ hypersurface Journal of the American Chemical Society. 121: 11531-11537. DOI: 10.1021/Ja9923639 |
0.715 |
|
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