Absolute stereochemistry of the strevertenes.

Chirality

Department of Chemistry, Columbia University, New York, NY 10027, USA.

Published: January 2000

The CD exciton chirality method was applied to determine the absolute stereochemistry of the strevertenes, antifungal pentaene macrolides produced by Streptoverticillium sp. LL-30F848. The CD difference spectrum of strevertene A methyl ester 15-dimethylaminobenzoate showed a positive couplet between the dimethylaminobenzoate and the pentaene chromophores, and therefore established the 15R configuration. Thus, by considering the relative configurations of the remaining stereogenic centers as derived from X-ray crystallography and ROESY experiments, the absolute stereochemistry of the strevertenes is established as 2R, 3S, 5S, 7S, 11R, 13R, 14R, 15R, 26S and 27R.

Download full-text PDF

Source
http://dx.doi.org/10.1002/(SICI)1520-636X(2000)12:1<43::AID-CHIR8>3.0.CO;2-NDOI Listing

Publication Analysis

Top Keywords

absolute stereochemistry
12
stereochemistry strevertenes
12
strevertenes exciton
4
exciton chirality
4
chirality method
4
method applied
4
applied determine
4
determine absolute
4
strevertenes antifungal
4
antifungal pentaene
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!