Synthesis of ring A of ambruticin and proof of its absolute stereochemistry
- 15 October 1980
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 58 (20) , 2173-2177
- https://doi.org/10.1139/v80-348
Abstract
Appropriately derivatized ambruticin was converted by reductive ozonolysis to tetrahydropyran 9c and cyclopropane 12a, which were synthesized from L-arabinose and (R)-Feist''s acid in an unambiguous manner.This publication has 1 reference indexed in Scilit:
- W-7783, a unique antifungal antibioticThe Journal of Organic Chemistry, 1977