One-step synthesis of azepino[3,4-<i>b</i>]indoles by cooperative aza-[4 + 3] cycloaddition from readily available feedstocks-Reference-Cited by-同舟云学术

One-step synthesis of azepino[3,4-b]indoles by cooperative aza-[4 + 3] cycloaddition from readily available feedstocks

Published:2022 Issue:17 Volume:9 Page:4640-4648
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Ma Jin-Tian¹,Chen Ting¹,Chen Xiang-Long¹,Zhou You¹,Yu Zhi-Cheng¹,Zhuang Shi-Yi¹,Alimu Maierhaba¹,Wu Yan-Dong¹,Xiang Jia-Chen²^ORCID,Wu An-Xin¹^ORCID

Affiliation:

1. Key Laboratory of Pesticide & Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, Wuhan 430079, P. R. China

2. School of Chemistry and Chemical Engineering, Southeast University, Nanjing 211189, China

Abstract

We demonstrate the feasibility of obtaining azepino[3,4-b]indoles by one-step synthesis from a four-component reaction system comprising readily available starting materials. This transformation affords a diverse range of azepino[3,4-b]indoles in a highly efficient manner.

Funder

Fundamental Research Funds for the Central Universities

Higher Education Discipline Innovation Project

Natural Science Foundation of Jiangsu Province

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/QO/D2QO00816E

Reference75 articles.