| Literature DB >> 22443275 |
Luiz C Dias1, Marco A B Ferreira.
Abstract
A stereoselective total synthesis of the reported structure of goniotrionin (4) has been accomplished. The key steps involved the opening of a chiral epoxide, a highly diastereoselective Mukaiyama aerobic oxidative cyclization, a selective 1,2-syn Mukaiyama aldol reaction, and a Noyori reduction.Entities:
Mesh:
Substances:
Year: 2012 PMID: 22443275 DOI: 10.1021/jo3004106
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354