Issue 3, 1987

The intermediacy of trichloromethyl anions in the reaction of enamines with bromotrichloromethane

Abstract

Reaction of N-(cyclohex-1-enyl)pyrrolidine with bromotrichloromethane in dimethyl sulphoxide generates trichloromethyl anions which have been trapped by addition to iminium cations or converted into chloroform in the presence of a hydrogen ion source.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 216-217

The intermediacy of trichloromethyl anions in the reaction of enamines with bromotrichloromethane

S. Löfås and P. Ahlberg, J. Chem. Soc., Chem. Commun., 1987, 216 DOI: 10.1039/C39870000216

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