The purpose of our work is to develop new methodology for the synthesis of biologically active polyether antibiotics. The work proposed involves the chelation-directed addition of organometallics to alkoxycarbonyl compounds and macrocyclically-directed remote asymmetric induction. Such methodology is being applied to the total synthesis of the polyether antibiotics monensin and lysocellin.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL025634-06
Application #
3338152
Study Section
Medicinal Chemistry Study Section (MCHA)
Project Start
1980-04-01
Project End
1988-03-31
Budget Start
1985-04-01
Budget End
1986-03-31
Support Year
6
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Columbia University (N.Y.)
Department
Type
Graduate Schools
DUNS #
064931884
City
New York
State
NY
Country
United States
Zip Code
10027
Carrasco, M R; Still, W C (1995) Engineering of a synthetic receptor to alter peptide binding selectivity. Chem Biol 2:205-12
Bhagwat, S S; Hamann, P R; Still, W C et al. (1985) Synthesis and structure of the platelet aggregation factor thromboxane A2. Nature 315:511-3