Issue 11, 1972

Alkene formation via aluminium trichloride-induced elimination from benzyl alkoxides

Abstract

Alkenes have been prepared by elimination from benzyl alkoxides, leading to anti-Saytzeff products; the mechanism is discussed on the basis of the products formed and of an observed hydrogen–deuterium isotope effect.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 679-680

Alkene formation via aluminium trichloride-induced elimination from benzyl alkoxides

T. J. Mead, G. Cum and N. Uccella, J. Chem. Soc., Chem. Commun., 1972, 679 DOI: 10.1039/C39720000679

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