Nickel/photoredox dual-catalyzed reductive cross-coupling of aryl halides and aldehydes-Reference-Cited by-同舟云学术

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Nickel/photoredox dual-catalyzed reductive cross-coupling of aryl halides and aldehydes

Published:2024 Issue:4 Volume:11 Page:1205-1210
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Liu Junjie¹,Chen Yukun¹,Zhao Hongping¹,Yuan Weiming¹²^ORCID

Affiliation:

1. Key Laboratory of Material Chemistry for Energy Conversion and Storage, Ministry of Education, Hubei Key Laboratory of Bioinorganic Chemistry and Materia Medica, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology (HUST), 1037 Luoyu Road, Wuhan 430074, PR China

2. Shenzhen Huazhong University of Science and Technology Research Institute, Shenzhen 518000, PR China

Abstract

A photoredox-assisted nickel-catalyzed reductive coupling of aryl halides and aldehydes to afford silyl-protected alcohols is reported. Key to success of this strategy is to identify α-silylamines as efficient organic reductants.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D3QO01927F

Reference44 articles.

1. Comprehensive Organic Synthesis , ed. P. Knochel and G. A. Molander , Elsevier , Oxford , 2nd edn, 2014 , vol. 1 and 2

2. Modern Arylation Methods , ed. L. Ackermann , Wiley-VCH , Weinheim , 2009

3. G. S.Silverman and P. E.Rakita , Handbook of Grignard-Reagents , Marcel Dekker , New York , 1996

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