Direct α-heteroarylation of amides (α to nitrogen) and ethers through a benzaldehyde-mediated photoredox reaction-Reference-Cited by-同舟云学术

Direct α-heteroarylation of amides (α to nitrogen) and ethers through a benzaldehyde-mediated photoredox reaction

Published:2016 Issue:3 Volume:7 Page:2111-2118
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Zhang Yongqiang¹²³⁴⁵,Teuscher Kevin B.¹²³⁴⁵,Ji Haitao¹²³⁴⁵^ORCID

Affiliation:

1. Department of Chemistry

2. Center for Cell and Genome Science

3. University of Utah

4. Salt Lake City

5. USA

Abstract

A benzaldehyde-mediated photoredox reaction for the α-heteroarylation of amides (α to nitrogen) and ethers through cross-dehydrogenative coupling (CDC).

Funder

Congressionally Directed Medical Research Programs

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/SC/C5SC03640B

Reference49 articles.

1. Recent Developments of Free-Radical Substitutions of Heteroaromatic Bases

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4. Direct Sp3α-C–H activation and functionalization of alcohol and ether

5. Direct C2-Alkylation of Azoles with Alcohols and Ethers through Dehydrogenative Cross-Coupling under Metal-Free Conditions

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