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Facile access to S-aryl/alkyl dithiocarbamates via a three-component reaction under metal-free conditions.
Xu, Lin-Lin; Wang, Si-Ran; Sun, Jia-Qi; Zhang, Ren-Jia; Tong, Jun; Xu, Da-Zhen.
Afiliação
  • Xu LL; National Engineering Research Center of Pesticide, College of Chemistry, Nankai University, Tianjin 300071, China. xudazhen@nankai.edu.cn.
  • Wang SR; National Engineering Research Center of Pesticide, College of Chemistry, Nankai University, Tianjin 300071, China. xudazhen@nankai.edu.cn.
  • Sun JQ; National Engineering Research Center of Pesticide, College of Chemistry, Nankai University, Tianjin 300071, China. xudazhen@nankai.edu.cn.
  • Zhang RJ; National Engineering Research Center of Pesticide, College of Chemistry, Nankai University, Tianjin 300071, China. xudazhen@nankai.edu.cn.
  • Tong J; National Engineering Research Center of Pesticide, College of Chemistry, Nankai University, Tianjin 300071, China. xudazhen@nankai.edu.cn.
  • Xu DZ; National Engineering Research Center of Pesticide, College of Chemistry, Nankai University, Tianjin 300071, China. xudazhen@nankai.edu.cn.
Org Biomol Chem ; 22(37): 7702-7706, 2024 Sep 25.
Article em En | MEDLINE | ID: mdl-39224970
ABSTRACT
The development of facile and convenient atom-economical methods for the preparation of organosulfur compounds from CS2 is a challenging endeavor. Herein, a one-pot, environmentally friendly method to access S-aryl/alkyl dithiocarbamates has been demonstrated by a three-component coupling involving aryl/alkyl thiols, CS2 and amines in the presence of a common base K2CO3. The transformation process can proceed in an H2O-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.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Biomol Chem Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Biomol Chem Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China País de publicação: Reino Unido