Iodine‐Mediated Regioselective Radical Cyclization of <i>o</i>‐Vinylaryl Isocyanides with Disulfides/Diselenides Leading to 2‐Chalcogenated Quinolines-Reference-Cited by-同舟云学术

Iodine‐Mediated Regioselective Radical Cyclization of o‐Vinylaryl Isocyanides with Disulfides/Diselenides Leading to 2‐Chalcogenated Quinolines

Published:2023-10-02 Issue:22 Volume:365 Page:3814-3818
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv Synth Catal

Author:

Li Ya‐Nan¹,Chen Fan¹,Zhang Xing‐Guo¹^ORCID,Tu Hai‐Yong¹^ORCID

Affiliation:

1. College of Chemistry and Materials Engineering Wenzhou University Wenzhou 325035 People's Republic of China

Abstract

AbstractAn iodine‐mediated radical cyclization of o‐vinylaryl isocyanides with disulfides or diselenides was developed. The atom‐economic reaction provides a method for regioselective construction of the 2‐chalcogenated quinolines in 42–93% yields by incorporation of both chalcogen atoms of disulfides or diselenides into quinolines.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202300777

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