Selective N–N or N–S bond cleavage of 1-trifluoromethyl benzotriazoles enables divergent synthesis of 1,2,4-benzotriazines and benzotriazoles-Reference-Cited by-同舟云学术

Selective N–N or N–S bond cleavage of 1-trifluoromethyl benzotriazoles enables divergent synthesis of 1,2,4-benzotriazines and benzotriazoles

Published:2023 Issue:20 Volume:10 Page:5138-5143
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Wang Xinyuan¹,Shan Yueyue¹,Mao Hui¹,Xiao Xiao²^ORCID,Wang Nengzhong³^ORCID,Lv Xin¹^ORCID,Zhou Liejin¹^ORCID

Affiliation:

1. Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, Department of Chemistry, Zhejiang Normal University, 688 Yingbin Road, Jinhua 321004, P. R. China

2. Institute of Pharmaceutical Science and Technology, Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, Zhejiang University of Technology, Hangzhou 310014, China

3. Hubei Key Laboratory of Natural Products Research and Development, College of Biological and Pharmaceutical Sciences, China Three Gorges University, Yichang 443002, China

Abstract

A variety of 1,2,4-benzotriazines and benzotriazoles are conveniently and divergently synthesized via selective N–N or N–S bond cleavage of 1-trifluoromethyl benzotriazoles under different basic conditions.

Funder

National Natural Science Foundation of China

Department of Education of Zhejiang Province

Natural Science Foundation of Zhejiang Province

Natural Science Foundation of Hubei Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/QO/D3QO00916E

Reference66 articles.