Issue 12, 1972

Kinetics of nucleophilic substitution of α-halogeno-sulphoxides

Abstract

α-Halogenomethyl sulphoxides react with PrnO and EtS in PrnOH via SN2 substitution; α0halogenoethyl and isopropyl derivatives react more slowly: SN2 reactions are greatly retarded by steric effects and SN1 reactions by the effect of the SO group.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 734-735

Kinetics of nucleophilic substitution of α-halogeno-sulphoxides

M. Cinquini, D. Landini and A. Maia, J. Chem. Soc., Chem. Commun., 1972, 734 DOI: 10.1039/C39720000734

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