Photo‐Driven Direct C−H Arylation of Quinoxalin‐2(1<i>H</i>)‐Ones with Aryltriazenes under Catalyst‐Free and Ambient Conditions-Reference-Cited by-同舟云学术

Photo‐Driven Direct C−H Arylation of Quinoxalin‐2(1H)‐Ones with Aryltriazenes under Catalyst‐Free and Ambient Conditions

Published:2023-03-02 Issue:13 Volume:26 Page:
ISSN:1434-193X
Container-title:European Journal of Organic Chemistry
language:en
Short-container-title:Eur J Org Chem

Author:

Wang Bin¹,Feng Yun¹,Zhang Yuepan¹,Wang Shoucai¹,Zhou Xinlei¹,Chen Ziren¹,Xia Yu¹,Jin Weiwei¹,Iqbal Azhar²,Liu Chenjiang¹,Zhang Yonghong¹^ORCID

Affiliation:

1. Urumqi Key Laboratory of Green Catalysis and Synthesis Technology Key Laboratory of Oil and Gas Fine Chemicals Ministry of Education & Xinjiang Uygur Autonomous Region State Key Laboratory of Chemistry and Utilization of Carbon Based Energy Resources College of Chemistry Xinjiang University 830046 Urumqi P. R. China

2. Department of Chemistry Bacha Khan University 24420 Charsadda Pakistan

Abstract

AbstractA photo‐induced direct arylation of quinoxalin‐2(1H)‐ones with aryltriazenes under catalyst‐free and ambient conditions was developed. The synthetic importance of this methodology was showcased by the simple operation, good functional group tolerance, and gram‐scale synthesis.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.202300044

Reference81 articles.

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3. Design, Synthesis, and Biological Activity of Potent and Selective Inhibitors of Blood Coagulation Factor Xa

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5. Prolyl Oligopeptidase Inhibition by N-Acyl-pro-pyrrolidine-type Molecules

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