Mark S. Kerr, Ph.D. - Publications

Affiliations: 
2007 Colorado State University, Fort Collins, CO 
Area:
Organic Chemistry, Catalysis

7 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
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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