| Literature DB >> 16408911 |
Paul A Roethle1, Dirk Trauner.
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.Entities:
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Year: 2006 PMID: 16408911 DOI: 10.1021/ol052922i
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005