Issue 6, 1975

Long-chain enals via carbonyl–olefin metathesis. An application in pheromone synthesis

Abstract

7-Phenylhept-6-enal and non-6-enal have been obtained from readily avilable materials through consecutive photochemical cycloaddition and selective thermal cycloreversion steps involving bicyclic oxetans as intermediates; subsequent reduction in one of the series produces trans-non-6-en-1-ol, an insect pheromone.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1975, 206-207

Long-chain enals via carbonyl–olefin metathesis. An application in pheromone synthesis

G. Jones, M. A. Acquadro and M. A. Carmody, J. Chem. Soc., Chem. Commun., 1975, 206 DOI: 10.1039/C39750000206

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