Regioselective intramolecular cyclization of <i>o</i>-alkynyl arylamines with the <i>in situ</i> formation of ArXCl to construct poly-functionalized 3-selenylindoles-Reference-Cited by-同舟云学术

Regioselective intramolecular cyclization of o-alkynyl arylamines with the in situ formation of ArXCl to construct poly-functionalized 3-selenylindoles

Published:2023 Issue:9 Volume:13 Page:6210-6216
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Yu Minhui¹²,Jin Tao¹,Wang Xiaohua³,Li Haohu¹,Ji Decai¹,Yao Jinzhong²^ORCID,Zeng Heyang¹,Shi Senlei¹,Xu Kaimeng¹,Zhang Lianpeng¹^ORCID

Affiliation:

1. Yunnan Provincial Key Laboratory of Wood Adhesives and Glued Products, Southwest Forestry University, Kunming 650224, Yunnan, China

2. College of Biological, Chemical Sciences and Engineering, Jiaxing University, Jiaxing 314001, Zhejiang, China

3. Tongji Zhejiang College, Jiaxing 314051, China

Abstract

In this paper, we have developed a metal-free protocol for the controllable synthesis of various 3-selenyl/sulfenyl/telluriumindoles from the regioselective intramolecular cyclization reactions of in situ generated RXCl with o-alkynyl arylamines.

Funder

National Natural Science Foundation of China

Department of Education of Zhejiang Province

Natural Science Foundation of Zhejiang Province

Southwest Forestry University

Higher Education Discipline Innovation Project

Yunnan Provincial Department of Education

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

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