Enantioselective synthesis of the C1,6-C21,16 segment of macbecins I and II
- 1 January 1989
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- No. 1,p. 190-192
- https://doi.org/10.1039/p19890000190
Abstract
A highly efficient and stereocontrolled enantioselective synthesis of the C1,6-C21,16segment of macbecins I and II has been performed in 19 steps and 28.5% overall yield.This publication has 1 reference indexed in Scilit:
- Herbimycin, a new antibiotic produced by a strain of Streptomyces.The Journal of Antibiotics, 1979