Journal of Organometallic Chemistry

Alkylation des carbenoides par des nucleophiles: I. Alkylation de carbenoides α esters et α phosphonates par des cuprates symetriques et dissymetriques

J Villieras, A Reliquet, JF Normant

文献索引：Villieras,J. et al. Journal of Organometallic Chemistry, 1978 , vol. 144, p. 17 - 25

全文：HTML全文

被引用次数: 12

摘要

Abstract The electrophilic character of carbenoïds can be activated by addition of organocopper reagents (RCu, R 2 CuM, or RCuZM), forming an unsymmetrical cuprate. Internal substitution of the carbenoïd halogen by the R group leads to a new alkylated unsymmetrical cuprate reagent. R can be primary, secondary, or tertiary alkyl, aryl, thiophenyl.