Visible light-driven dearomative ring expansion of (aza)arenes to access dihydrofuran-based polycyclic compounds-Reference-Cited by-同舟云学术

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Visible light-driven dearomative ring expansion of (aza)arenes to access dihydrofuran-based polycyclic compounds

Published:2024 Issue:23 Volume:15 Page:8828-8834
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Zhang Linghong¹,You Mengdi²,Ban Xu²,Zhao Xiaowei¹,Yin Yanli²,Cao Shanshan²,Jiang Zhiyong¹²^ORCID

Affiliation:

1. Key Laboratory of Natural Medicine and Immuno-Engineering of Henan Province, Henan University, Kaifeng, Henan, P. R. China, 475004

2. School of Chemistry and Chemical Engineering, Pingyuan Laboratory, Henan Normal University, Xinxiang, Henan, P. R. China, 453007

Abstract

A visible light-mediated dearomative ring expansion strategy that is general as the good compatibility of diverse arenes and azaarenes have been developed.

Funder

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Henan Key Laboratory of Organic Functional Molecules and Drug Innovation

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/SC/D4SC00748D

Reference32 articles.

1. Green chemistry for chemical synthesis

2. Ueber die Einwirkung von salpetriger Säure auf salzsauren Glycocolläther

3. Transition-metal-catalyzed reactions of diazo compounds. 2. Addition to aromatic molecules: catalysis of Buchner's synthesis of cycloheptatrienes

4. Regioselective and Enantioselective Intermolecular Buchner Ring Expansions in Flow

5. Catalytic, Asymmetric Dearomative Synthesis of Complex Cyclohexanes via a Highly Regio- and Stereoselective Arene Cyclopropanation Using α-Cyanodiazoacetates

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