Single-step preparation of allylic sulfides having 1-phenyltetrazole-5-thio group from allylic alcohols using ,′-BIS(1-phenyl-1-tetrazol-5-YL) dithiocarbonate and reactions involving the allylic sulfides
作者:Kazuyoshi Takeda、Kanoko Tsuboyama、Katsumi Torii、Maki Murata、Haruo Ogura
DOI:10.1016/s0040-4039(00)80428-1
日期:1988.1
The reaction of allylic alcohols and ,′-bis(1-phenyl-1-tetrazol-5-yl) dithiocarbonate () gave allylic sulfides having 1-phenyltetrazole-5-thio group in a single step. Furthermore, these allylic sulfides could be applied to carbon-carbon bond and carbon-sulfur bond formations by using Grignard reagents or carbanions in the presence of a catalytic amount of copper(I)bromide or palladium (0), respectively
烯丙醇和的反应,双(1-苯基-1-四唑-5-基)二硫代碳酸酯(),得到具有在一个单一的步骤1苯基四唑基-5-硫代基烯丙基硫化物。此外,在催化量的溴化铜(I)或钯(0)的存在下,分别使用格氏试剂或碳负离子,可以将这些烯丙基硫化物应用于碳-碳键和碳-硫键的形成。