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Recent advances in the radical cascade reaction for constructing nitrogen heterocycles using azides as radical acceptors.
Xia, Dong; Shi, Yun; Jiang, Liying; Li, Yang; Kong, Jianfei.
Afiliação
  • Xia D; College of Pharmacy, Jiangsu Vocational College of Medicine, Yancheng, 224005, P. R. China. jsmcxd@163.com.
  • Shi Y; College of Pharmacy, Jiangsu Vocational College of Medicine, Yancheng, 224005, P. R. China. jsmcxd@163.com.
  • Jiang L; College of Pharmacy, Jiangsu Vocational College of Medicine, Yancheng, 224005, P. R. China. jsmcxd@163.com.
  • Li Y; School of Bioengineering, Huainan Normal University, Huainan, 232038, P. R. China. yangli@hnnu.edu.cn.
  • Kong J; College of Pharmacy, Jiangsu Vocational College of Medicine, Yancheng, 224005, P. R. China. jsmcxd@163.com.
Org Biomol Chem ; 22(27): 5511-5523, 2024 Jul 10.
Article em En | MEDLINE | ID: mdl-38904322
ABSTRACT
Due to the high conversion properties, azide compounds are widely utilized in organic synthesis. For instance, azide compounds readily release nitrogen to form a new N-C bond when they function as radical acceptors for the active intermediates in the reaction. Over the past decade, strategies employing azides as radical acceptors to construct nitrogen heterocycles have been extensively developed. This approach has emerged as a crucial method for synthesizing nitrogen heterocycles. Therefore, this paper provides a review of the research advancements in tandem cyclization reactions using azides as radical acceptors, summarizing the process of reaction design, exploration, reasoning of the mechanism, and prospects for further research of these reactions.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article