Visible light-induced radical cyclization of <i>o</i>-alkenyl aromatic isocyanides with thioethers: direct synthesis of 2-thioquinolines-Reference-Cited by-同舟云学术

Visible light-induced radical cyclization of o-alkenyl aromatic isocyanides with thioethers: direct synthesis of 2-thioquinolines

Published:2024 Issue:7 Volume:11 Page:2033-2039
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Liang Yong-Xin¹²,Gong Yue¹,Xu Xue-Cen¹,Yang Ming¹,Zhao Yu-Long¹^ORCID

Affiliation:

1. Jilin Province Key Laboratory of Organic Functional Molecular Design & Synthesis, Faculty of Chemistry, Northeast Normal University, Changchun 130024, China

2. College of Chemistry and Chemical Engineering Qilu Normal University, Jinan 250200, China

Abstract

A novel visible-light-induced regioselective radical cyclization reaction of isocyanides with thioethers has been developed. This reaction provides an efficient method for the construction of highly functionalized quinolines in a single step.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D3QO02055J

Reference68 articles.

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3. 4-Substituted Thioquinolines and Thiazoloquinolines: Potent, Selective, and Tween-80 in vitro Dependent Families of Antitubercular Agents with Moderate in vivo Activity

4. 8-Aminoquinoline: A Powerful Directing Group in Metal-Catalyzed Direct Functionalization of CH Bonds

5. Ligand-Enabled Pd(II)-Catalyzed Bromination and Iodination of C(sp3)–H Bonds

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