Issue 22, 1982

Reaction of 2-alkyl-2-phenyl-1,3-dioxolans with iodine monochloride: formation of α-phenylalkanoate esters

Abstract

2-Alkyl-2-phenyl-1,3-dioxolans undergo a high-yield transformation into 2-chloroethyl α-phenylalkanoates upon treatment with iodine monochloride in dichloromethane.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1982, 1311-1312

Reaction of 2-alkyl-2-phenyl-1,3-dioxolans with iodine monochloride: formation of α-phenylalkanoate esters

A. Goosen and C. W. McCleland, J. Chem. Soc., Chem. Commun., 1982, 1311 DOI: 10.1039/C39820001311

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