Issue 0, 1987

Applications of the stereochemically-controlled Horner-Wittig reaction: synthesis of feniculin, (E)-non-6-en-1-ol, a pheromone of the mediterranean fruit fly, (E)- and (Z)-dec-5-en-1-ol, tri-substituted alkenes, and (Z)-α-bisabolene

Abstract

Stereoselective reduction of the appropriate α-diphenylphosphinoyl ketone or addition of the lithium derivative of an alkyl diphenylphosphine oxide to an aldehyde or a ketone gives Horner-Wittig intermediates and hence the title compounds.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1987, 2569-2577

Applications of the stereochemically-controlled Horner-Wittig reaction: synthesis of feniculin, (E)-non-6-en-1-ol, a pheromone of the mediterranean fruit fly, (E)- and (Z)-dec-5-en-1-ol, tri-substituted alkenes, and (Z)-α-bisabolene

A. D. Buss, N. Greeves, R. Mason and S. Warren, J. Chem. Soc., Perkin Trans. 1, 1987, 2569 DOI: 10.1039/P19870002569

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