Mark S. Kerr, Ph.D. - Publications
Affiliations: | 2007 | Colorado State University, Fort Collins, CO |
Area:
Organic Chemistry, CatalysisYear | Citation | Score | |||
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2010 | Vora HU, Lathrop SP, Reynolds NT, Kerr MS, De Alaniz JR, Rovis T, Chennamadhavuni S, Davies HML. Preparation of chiral and achiral triazolium salts: Carbene precursors with demonstrated synthetic utility Organic Syntheses. 87: 350-361. DOI: 10.1002/0471264229.Os087.37 | 0.504 | |||
2008 | de Alaniz JR, Kerr MS, Moore JL, Rovis T. Scope of the asymmetric intramolecular stetter reaction catalyzed by chiral nucleophilic triazolinylidene carbenes. The Journal of Organic Chemistry. 73: 2033-40. PMID 18302407 DOI: 10.1021/Jo702313F | 0.709 | |||
2006 | Moore JL, Kerr MS, Rovis T. Enantioselective formation of quaternary stereocenters using the catalytic intramolecular Stetter reaction Tetrahedron. 62: 11477-11482. DOI: 10.1016/J.Tet.2006.06.042 | 0.706 | |||
2005 | Kerr MS, Read de Alaniz J, Rovis T. An efficient synthesis of achiral and chiral 1,2,4-triazolium salts: bench stable precursors for N-heterocyclic carbenes. The Journal of Organic Chemistry. 70: 5725-8. PMID 15989360 DOI: 10.1021/Jo050645N | 0.71 | |||
2004 | Kerr MS, Rovis T. Enantioselective synthesis of quaternary stereocenters via a catalytic asymmetric Stetter reaction. Journal of the American Chemical Society. 126: 8876-7. PMID 15264801 DOI: 10.1021/Ja047644H | 0.716 | |||
2003 | Kerr MS, Rovis T. Effect of the Michael Acceptor in the Asymmetric Intramolecular Stetter Reaction Synlett. 1934-1936. DOI: 10.1055/S-2003-41458 | 0.675 | |||
2002 | Kerr MS, Read de Alaniz J, Rovis T. A highly enantioselective catalytic intramolecular Stetter reaction. Journal of the American Chemical Society. 124: 10298-9. PMID 12197730 DOI: 10.1021/Ja027411V | 0.71 | |||
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