Expedient synthesis of (+/-)-bipinnatin J
- PMID: 16408911
- DOI: 10.1021/ol052922i
Expedient synthesis of (+/-)-bipinnatin J
Abstract
[reaction: see text] A nine-step, stereoselective synthesis of bipinnatin J is described, which features a ruthenium-catalyzed Alder-ene reaction, a Stille cross coupling, and an intramolecular Nozaki-Hiyama-Kishi allylation as key steps. The biosynthetic relationship between bipinnatin J and complex polycyclic diterpenes isolated from gorgonian corals is discussed.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
