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一步两步一锅法将苯乙烯进行二硫代氨基甲酰化:无金属立体选择性合成苯乙烯基二硫代氨基甲酸盐。

One-pot two-step dithiocarbamylation of styrenes: metal-free stereoselective synthesis of styrenyl dithiocarbamates.

机构信息

Department of Chemistry, Jadavpur University, Kolkata 700032, India.

出版信息

Org Biomol Chem. 2022 May 4;20(17):3491-3494. doi: 10.1039/d2ob00315e.

Abstract

Styrenes have been functionalized to produce styrenyl dithiocarbamates by a one-pot two-step procedure without using any metal catalysts. Styrene was transformed into a bromo-derivative, which undergoes a domino nucleophilic substitution followed by elimination in the presence of a dithiocarbamate anion and triethylamine to produce -styrenyl dithiocarbamates exclusively. The reaction shows a wide substrate scope and good yields of products.

摘要

苯乙烯通过一锅两步法进行功能化,得到苯乙烯基二硫代氨基甲酸盐,无需使用任何金属催化剂。苯乙烯被转化为溴代衍生物,在二硫代氨基甲酸盐阴离子和三乙胺的存在下,通过多米诺亲核取代和消除反应,生成 - 苯乙烯基二硫代氨基甲酸盐。该反应具有广泛的底物范围和良好的产物收率。

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