Photoinduced C–H arylation of 1,3-azoles <i>via</i> copper/photoredox dual catalysis-Reference-Cited by-同舟云学术

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Photoinduced C–H arylation of 1,3-azoles via copper/photoredox dual catalysis

Published:2024 Issue:19 Volume:15 Page:7293-7299
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Trienes Sven¹²^ORCID,Xu Jiawei¹,Ackermann Lutz¹²^ORCID

Affiliation:

1. Institut für Organische und Biomolekulare Chemie, Wöhler Research Institute for Sustainable Chemistry (WISCh), Georg-August-Universität, Tammannstraße 2, 37077 Göttingen, Germany

2. DZHK (German Centre for Cardiovascular Research), Potsdamer Straße 58, 10875 Berlin, Germany

Abstract

The photo-induced azole C–H arylation was realized with a dual-catalytic copper-based system. Exceedingly mild reaction conditions at ambient temperature and visible light irradiation enabled a broad scope with high functional group tolerance.

Funder

Deutsches Zentrum für Herz-Kreislaufforschung

HORIZON EUROPE European Research Council

Deutsche Forschungsgemeinschaft

China Scholarship Council

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/SC/D4SC00393D

Reference70 articles.

1. Mild metal-catalyzed C–H activation: examples and concepts

2. C–H activation

3. Enantioselective C H Bond Functionalizations by 3d Transition-Metal Catalysts

4. Arene diversification through distal C(sp 2 )−H functionalization

5. Transition Metal-Catalyzed C–H Amination: Scope, Mechanism, and Applications

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Defluorinative Haloalkylation of Unactivated Alkenes Enabled by Dual Photoredox and Copper Catalysis;The Journal of Organic Chemistry;2024-09-10

2. Dual Copper Photoredox C–H Alkynylation with Arylacetylenes;Organic Letters;2024-09-10

3. Photo-Induced Copper-Catalyzed C–H Arylation of 1,3-Azoles;Synfacts;2024-06-14

4. Regiodivergent C–H alkynylation of 2-arylthiazoles switched by Ru^II and Pd^II catalysis;Chemical Communications;2024

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