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Issue 16, 1990
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A versatile and convenient method for the preparation of α-(Z)-1-alkenyl ketones from β-keto benzyl esters

Abstract

A versatile and selective method for the preparation of α-(Z)-1-alkenyl ketones from -keto benzyl esters has been developed by exploiting the three-step sequence of an improved Pinhey's alkynylation, semihydrogenation, and reductive debenzyloxycarbonylation.

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Article information


J. Chem. Soc., Chem. Commun., 1990, 1100-1102
Article type
Paper

A versatile and convenient method for the preparation of α-(Z)-1-alkenyl ketones from β-keto benzyl esters

S. Hashimoto, Y. Miyazaki, T. Shinoda and S. Ikegami, J. Chem. Soc., Chem. Commun., 1990, 1100
DOI: 10.1039/C39900001100

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