Kevin M. Peese, Ph.D.

Affiliations: 
2007 University of Illinois, Urbana-Champaign, Urbana-Champaign, IL 
Area:
Organic Chemistry, Natural Product Synthesis, Medicinal Chemistry
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David Y. Gin grad student 2007 UIUC
 (Asymmetric total synthesis of (+)-nominine: Development of a dual cycloaddition strategy for the synthesis of the hetisine alkaloids.)
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Peese KM, Gin DY. (2013) Nominine Total Synthesis of Natural Products: At the Frontiers of Organic Chemistry. 1-24
Peese KM, Gin DY. (2008) Asymmetric synthetic access to the hetisine alkaloids: total synthesis of (+)-nominine. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 1654-65
Peese KM, Gin DY. (2006) Efficient synthetic access to the hetisine C20-diterpenoid alkaloids. A concise synthesis of nominine via oxidoisoquinolinium-1,3-dipolar and dienamine-Diels-Alder cycloadditions. Journal of the American Chemical Society. 128: 8734-5
McClure KF, Letavic MA, Kalgutkar AS, et al. (2006) Structure-activity relationships of triazolopyridine oxazole p38 inhibitors: identification of candidates for clinical development. Bioorganic & Medicinal Chemistry Letters. 16: 4339-44
Gin D, Peese K. (2006) Synthesis of (±)-Nominine Synfacts. 2006: 1206-1206
Peese KM, Gin DY. (2005) Enantioselective approach to the hetisine alkaloids. Synthesis of the 3-methyl-1-aza-tricyclo[5.2.1.0(3,8)]decane core via intramolecular dipolar cycloaddition. Organic Letters. 7: 3323-5
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