烷基
化学
试剂
硫醇
催化作用
卤化物
铜
基质(水族馆)
组合化学
硫化物
有机化学
海洋学
地质学
作者
Qingqiang Tian,Lili Wang,Yahui Li
标识
DOI:10.1080/17415993.2021.1967354
摘要
A new and convenient copper-catalyzed synthesis of alkyl sulfides has been accomplished using S-alkyl butanethioate as a thiol source. This catalytic protocol displayed a good functional groups tolerance and high efficiency. Both secondary and primary alkyl iodides can be used in this procedure. In addition, this method features operational simplicity and a wide substrate range, providing a complementary method for alkyl sulfide synthesis without requiring toxic thiols and noble metals.
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