Indirect electrochemical reductive cyclization of<i>o</i>-halophenylacrylamides mediated by phenanthrene-Reference-Cited by-同舟云学术

Indirect electrochemical reductive cyclization ofo-halophenylacrylamides mediated by phenanthrene

Published:2023 Issue:8 Volume:10 Page:2039-2044
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Zhou Xue-Qi¹^ORCID,Chen Pei-Bo¹,Xia Qiang¹^ORCID,Xiong Ting-Kai¹^ORCID,Li Xue-Jun¹,Pan Ying-Ming²^ORCID,He Mu-Xue³^ORCID,Liang Ying¹^ORCID

Affiliation:

1. School of Life and Environmental Sciences, Guilin University of Electronic Technology, Guilin, Guangxi, 541004, People's Republic of China

2. State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmaceutical Sciences of Guangxi Normal University, Guilin 541004, People's Republic of China

3. Guangxi Key Laboratory of Environmental Exposomics and Entire Lifecycle Health, School of Public Health of Guilin Medical University, Guilin 541199, Guangxi, P. R. China

Abstract

We report a synthesis method for the selective 6-endocyclization ofo-phenylacrylamides to obtain 3,4-dihydroquinolinonesviaaryl anions formed by two-electron reduction under electrochemistry using phenanthrene as the reduction mediator.

Funder

Natural Science Foundation of Guangxi Province

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/QO/D3QO00280B

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