| Literature DB >> 10987921 |
R A Pilli1, M M Victor, A de Meijere.
Abstract
The first asymmetric total synthesis of Aspinolide B (1), a new 10-membered lactone discovered by chemical screening methods in the cultures of Aspergillus ochraceus, has been accomplished. The key steps included a selective Felkin-type addition of TMS-acetylene to aldehyde 3a and a Nozaki-Hiyama-Kishi coupling reaction to build the required 10-membered ring. This synthesis confirmed the absolute stereochemistry of aspinolide B, established through Helmchen's method and corrected its previously reported specific optical rotation.Entities:
Mesh:
Substances:
Year: 2000 PMID: 10987921 DOI: 10.1021/jo000327i
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354