Preparation of 1,4,5‐Trisubstituted 5‐Acyl‐1,2,3‐triazoles by Selective Acylation between Copper(I)‐Carbon( sp ) and Copper(I)‐Carbon( sp  2 ) Bonds with Acyl Chlorides | Zendy

Wang Bo | Zendy; Liu Nan | Zendy; Shao Changwei | Zendy; Zhang Qun | Zendy; Wang Xinyan | Zendy; Hu Yuefei | Zendy

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Preparation of 1,4,5‐Trisubstituted 5‐Acyl‐1,2,3‐triazoles by Selective Acylation between Copper(I)‐Carbon( sp ) and Copper(I)‐Carbon( sp 2 ) Bonds with Acyl Chlorides

Author(s) -

Wang Bo,

Liu Nan,

Shao Changwei,

Zhang Qun,

Wang Xinyan,

Hu Yuefei

Publication year - 2013

Publication title -

advanced synthesis and catalysis

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.541

H-Index - 155

eISSN - 1615-4169

pISSN - 1615-4150

DOI - 10.1002/adsc.201300307

Subject(s) - chemistry , acylation , copper , carbon fibers , organic chemistry , combinatorial chemistry , catalysis , materials science , composite number , composite material

A one‐pot, three‐component method for preparation of 1,4,5‐trisubstituted 5‐acyl‐1,2,3‐triazoles has been developed based on a highly selective acylation of the copper(I)‐carbon( sp 2 ) bond with acyl chlorides in the presence of the copper(I)‐carbon( sp ) bond. The procedure is characterized by high efficiency and simple conditions.

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