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Electrochemical synthesis of vicinal azidoacetamides.
Yu, Yi; Yuan, Yaofeng; Ye, Ke-Yin.
Affiliation
  • Yu Y; Key Laboratory of Molecule Synthesis and Function Discovery (Fujian Province University), College of Chemistry, Fuzhou University, Fuzhou 350108, China. kyye@fzu.edu.cn.
  • Yuan Y; Key Laboratory of Molecule Synthesis and Function Discovery (Fujian Province University), College of Chemistry, Fuzhou University, Fuzhou 350108, China. kyye@fzu.edu.cn.
  • Ye KY; Key Laboratory of Molecule Synthesis and Function Discovery (Fujian Province University), College of Chemistry, Fuzhou University, Fuzhou 350108, China. kyye@fzu.edu.cn.
Chem Commun (Camb) ; 59(4): 422-425, 2023 Jan 05.
Article in En | MEDLINE | ID: mdl-36514900
ABSTRACT
Vicinal diamines are an important structural motif in bioactive natural products and pharmaceutical intermediates. Herein, an environmentally friendly and efficient electrochemical approach to azidoacetamides, as one variant of vicinal diamines, has been developed. This reaction features mild conditions and broad substrate scope, without the use of any chemical oxidant or transition-metal catalysts. The obtained vicinal azidoacetamides could be conveniently converted into various other vicinal diamine derivatives.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Diamines Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2023 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Diamines Language: En Journal: Chem Commun (Camb) Journal subject: QUIMICA Year: 2023 Document type: Article Affiliation country:
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