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Molybdenum-catalyzed deoxygenative heterocyclization of 2-nitroazobenzenes: a novel strategy for catalytic synthesis of 2-aryl-2H-benzo[d][1,2,3]triazoles.
Liu, Quanyun; Chu, Haoke; Mai, Junju; Yang, Haobing; Shen, Mei-Hua; Xu, Hua-Dong.
Afiliação
  • Liu Q; School of Pharmacy, Changzhou University, Changzhou, Jiangsu Province 213164, China. chu@cczu.edu.cn.
  • Chu H; School of Pharmacy, Changzhou University, Changzhou, Jiangsu Province 213164, China. chu@cczu.edu.cn.
  • Mai J; School of Pharmacy, Changzhou University, Changzhou, Jiangsu Province 213164, China. chu@cczu.edu.cn.
  • Yang H; School of Pharmacy, Changzhou University, Changzhou, Jiangsu Province 213164, China. chu@cczu.edu.cn.
  • Shen MH; School of Pharmacy, Changzhou University, Changzhou, Jiangsu Province 213164, China. chu@cczu.edu.cn.
  • Xu HD; School of Pharmacy, Changzhou University, Changzhou, Jiangsu Province 213164, China. chu@cczu.edu.cn.
Org Biomol Chem ; 22(5): 954-958, 2024 Jan 31.
Article em En | MEDLINE | ID: mdl-38205622
ABSTRACT
A novel strategy for the catalytic synthesis of 2-aryl-2H-benzo[d][1,2,3]triazoles bearing a wide range of functional groups in good to excellent yields by non-noble molybdenum-catalyzed deoxygenative heterocyclization of 2-nitroazobenzenes is described. The salient features of the transformation include the use of readily available substrates, valuable products and ease of scale-up. The mechanistic study indicates that the reaction occurred via double deoxygenation by the Mo(VI)/Mo(IV) catalytic cycle from 2-nitroazobenzene, through the formation of 2-aryl-2H-benzo[d][1,2,3]triazole-N1-oxide or nitrene intermediates.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article