Diacetyl as a “traceless” visible light photosensitizer in metal-free cross-dehydrogenative coupling reactions-Reference-Cited by-同舟云学术

Diacetyl as a “traceless” visible light photosensitizer in metal-free cross-dehydrogenative coupling reactions

Published:2019 Issue:19 Volume:10 Page:5018-5024
ISSN:2041-6520
Container-title:Chemical Science
language:en
Short-container-title:Chem. Sci.

Author:

Huang Chia-Yu¹²³⁴⁵^ORCID,Li Jianbin¹²³⁴⁵^ORCID,Liu Wenbo¹²³⁴⁵^ORCID,Li Chao-Jun¹²³⁴⁵^ORCID

Affiliation:

1. Department of Chemistry

2. FRQNT Centre for Green Chemistry and Catalysis

3. McGill University

4. Montreal

5. Canada

Abstract

Minisci alkylation is of prime importance for its applicability in functionalizing diverse heteroarenes, which are core structures in many bioactive compounds.

Funder

Canada Foundation for Innovation

Natural Sciences and Engineering Research Council of Canada

McGill University

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/SC/C8SC05631E

Reference82 articles.

1. Palladium-catalyzed difluoromethylthiolation of heteroaryl bromides, iodides, triflates and aryl iodides

2. Catalytic enantioselective Minisci-type addition to heteroarenes

3. New general and convenient sources of alkyl radicals, useful for selective syntheses

4. Photoredox-mediated Minisci C–H alkylation of N-heteroarenes using boronic acids and hypervalent iodine

5. Molecular Oxygen-Mediated Minisci-Type Radical Alkylation of Heteroarenes with Boronic Acids

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