Reaction of diazonium salts with transition metals—III
作者:K. Kikukawa、K. Nagira、F. Wada、T. Matsuda
DOI:10.1016/s0040-4020(01)97711-7
日期:1981.1
Palladium (0) catalyzed reactions of arenediazonium salts for arylation of aliphatic and cyclic olefins and allylic alcohols, styrene and ethyl acrylate were studied. Effects of the olefinic compounds and other reaction variables on the arylation were presented. Arylpalladiumspecies was proposed as the most plausible intermediated in this reaction.
A short and efficient synthetic sequence to produce a wide variety of 3-arylpiperidines from three simple building blocks is described. The key step is a palladium-catalyzed arylation of cyclopentene.