Issue 12, 1996

Stereoselective rearrangement of 5,6-epoxy carotenoid model compounds

Abstract

Carotenoids with novel acyclic tetrasubstituted olefinic and cyclopentyl end groups are obtained by Lewis acid-promoted stereoselective rearrangement of the epoxide end group of 5,6-epoxy carotenoids.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1996, 1337-1339

Stereoselective rearrangement of 5,6-epoxy carotenoid model compounds

Y. Yamano, C. Tode and M. Ito, J. Chem. Soc., Perkin Trans. 1, 1996, 1337 DOI: 10.1039/P19960001337

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