作者:J. Nishimura、N. Kawabata、J. Furukawa
DOI:10.1016/0040-4020(69)80006-2
日期:1969.1
prepared in 32–96% yield by the reaction of olefins with ethylidene iodide and diethylzinc. The reaction is electrophilic, and proceeds stereospecifically. In the case of the reaction with 1,2-disubstituted olefins, cis and trans olefins affords cyclopropane derivatives whose configurations with respect to the substituents from original olefins are cis and trans, respectively.
通过烯烃与亚乙基碘和二乙基锌的反应,已经制备了几种甲基环丙烷,产率为32-96%。该反应是亲电的,并且立体定向地进行。在与1,2-二取代的烯烃反应的情况下,顺式和反式烯烃提供环丙烷衍生物,其相对于来自原始烯烃的取代基的构型分别为顺式和反式。