Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
3R01GM038904-11S1
Application #
2179600
Study Section
Medicinal Chemistry Study Section (MCHA)
Project Start
1991-07-01
Project End
1998-06-30
Budget Start
1996-03-01
Budget End
1996-06-30
Support Year
11
Fiscal Year
1996
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Crimmins, Michael T; DeBaillie, Amy C (2006) Enantioselective total synthesis of bistramide A. J Am Chem Soc 128:4936-7
Crimmins, Michael T; Vanier, Grace S (2006) Enantioselective total synthesis of (+)-SCH 351448. Org Lett 8:2887-90
Crimmins, Michael T; Slade, David J (2006) Formal synthesis of 6-deoxyerythronolide B. Org Lett 8:2191-4
Crimmins, M T; Hauser, E B (2000) Synthesis of crossed [2 + 2] photocycloadducts: a novel approach to the synthesis of bridged bicyclic alkenes. Org Lett 2:281-4
Crimmins, M T; Emmitte, K A; Katz, J D (2000) Diastereoselective alkylations of oxazolidinone glycolates: a useful extension of the Evans asymmetric alkylation. Org Lett 2:2165-7