Chemical communications
A new route to furanoeremophilane sesquiterpenoids. Synthesis of (±)-6β-hydroxyeuryopsin
MS Shanmugham, JD White
Index: Shanmugham, M. Sundaram; White, James D. Chemical Communications, 2004 , # 1 p. 44 - 45
Full Text: HTML
Citation Number: 10
Abstract
The naturally occurring furanoeremophilane 6β-hydroxyeuryopsin was synthesized by a novel route which involved Stille coupling of a 2-furylstannane with a cyclohexylmethyl bromide, followed by intramolecular formylation of the furan to complete the tricyclic nucleus of the sesquiterpenoid.
Related Articles:
An enantioselective approach to furanoeremophilanes:(+)-9-oxoeuryopsin
[Mace, Laura H.; Shanmugham, M. Sundaram; White, James D.; Drew, Michael G. B. Organic and Biomolecular Chemistry, 2006 , vol. 4, # 6 p. 1020 - 1031]