作者:Akira Oku、Masaharu Iwamoto、Kenji Sanada、Manabu Abe
DOI:10.1016/s0040-4039(00)60864-x
日期:1992.11
Chloro(phenyl)carbene and diphenylcarbene reacted with cyclopropanone hemiacetals, cyclopropanols, and cyclopropanone cyanohydrins to give 4-phenylbutanoic acid derivatives. The mechanism was explained in terms of a homolytic process that the O-H group of cyclopropanols reacted as a formal H donor with carbenes.
氯(苯基)卡宾和二苯卡宾与环丙烷酮半缩醛,环丙醇和环丙烷酮氰醇反应生成4-苯基丁酸衍生物。根据均相分解过程解释了该机理,其中环丙醇的OH基团作为正式的H供体与碳烯反应。