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在无金属条件下通过三组分反应轻松获得芳基/烷基二硫代氨基甲酸盐。

Facile access to -aryl/alkyl dithiocarbamates a three-component reaction under metal-free conditions.

作者信息

Xu Lin-Lin, Wang Si-Ran, Sun Jia-Qi, Zhang Ren-Jia, Tong Jun, Xu Da-Zhen

机构信息

National Engineering Research Center of Pesticide, College of Chemistry, Nankai University, Tianjin 300071, China.

出版信息

Org Biomol Chem. 2024 Sep 25;22(37):7702-7706. doi: 10.1039/d4ob01203h.

Abstract

The development of facile and convenient atom-economical methods for the preparation of organosulfur compounds from CS is a challenging endeavor. Herein, a one-pot, environmentally friendly method to access -aryl/alkyl dithiocarbamates has been demonstrated by a three-component coupling involving aryl/alkyl thiols, CS and amines in the presence of a common base KCO. The transformation process can proceed in an HO-DMAc (3 : 1) mixed solvent without requiring any catalysts or extensive prefunctionalization of reactants. The protocol is operationally simple and affords dithiocarbamates with various moieties (including aryl, aliphatic, heteroaryl and alkenyl) in good yields.

摘要

开发简便且原子经济的从二硫化碳制备有机硫化合物的方法是一项具有挑战性的工作。在此,通过芳基/烷基硫醇、二硫化碳和胺在常见碱碳酸钾存在下的三组分偶联,展示了一种一锅法、环境友好的制备芳基/烷基二硫代氨基甲酸盐的方法。该转化过程可以在水-二甲基乙酰胺(3∶1)混合溶剂中进行,无需任何催化剂或反应物的广泛预官能化。该方法操作简单,能以良好的产率得到带有各种基团(包括芳基、脂肪族、杂芳基和烯基)的二硫代氨基甲酸盐。

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