Palladium-catalyzed oxidative amidation of quinoxalin-2(1H)-ones with acetonitrile: a highly efficient strategy toward 3-amidated quinoxalin-2(1H)-ones-Reference-Cited by-同舟云学术

Palladium-catalyzed oxidative amidation of quinoxalin-2(1H)-ones with acetonitrile: a highly efficient strategy toward 3-amidated quinoxalin-2(1H)-ones

Published:2019 Issue:4 Volume:17 Page:876-884
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Yuan Jinwei¹²³⁴⁵^ORCID,Liu Shuainan⁵⁶³⁴,Xiao Yongmei⁵⁶³⁴,Mao Pu⁵⁶³⁴,Yang Liangru⁵⁶³⁴^ORCID,Qu Lingbo⁵⁶³⁴⁷

Affiliation:

1. Engineering Technology Research Center for Grain & Oil Food

2. State Administration of Grain

3. Zhengzhou 450001

4. P. R. China

5. School of Chemistry & Chemical Engineering

6. Henan University of Technology

7. College of Chemistry and Molecular Engineering

Abstract

An efficient protocol for the synthesis of 3-amidated quinoxalin-2(1H)-ones has been developed via a palladium-catalyzed cross-coupling reaction of quinoxalin-2(1H)-ones with acetonitrile.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/OB/C8OB03061H

Reference71 articles.

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2. Synthesis of certain substituted quinoxalines as antimicrobial agents (part II)

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4. Synthesis and antimicrobial activity of certain novel quinoxalines

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