A visible light-induced deoxygenative amidation protocol for the synthesis of dipeptides and amides-Reference-Cited by-同舟云学术

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A visible light-induced deoxygenative amidation protocol for the synthesis of dipeptides and amides

Published:2024 Issue:16 Volume:11 Page:4449-4455
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Ren Ji-Wei¹^ORCID,Han Cheng-Shuai¹,Zhang Huai-Xin¹,Zhang Qing-Hao¹,Song Xian-Ting¹,Sun Jing-Hui¹

Affiliation:

1. College of Chemistry and Chemical Engineering, Taishan University, Tai'an, Shandong, 271000, P. R. China

Abstract

A green and sustainable visible light-mediated deoxygenative amidation protocol to generate acyl radicals from carboxylic acids was developed to efficiently synthesize dipeptides and amides.

Funder

Natural Science Foundation of Shandong Province

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D4QO00793J

Reference74 articles.

1. Peptide and Amide Bond-Containing Dendrimers

2. Key green chemistry research areas—a perspective from pharmaceutical manufacturers

3. Rethinking amide bond synthesis

4. Analysis of Past and Present Synthetic Methodologies on Medicinal Chemistry: Where Have All the New Reactions Gone?

5. Direct and Chemoselective Synthesis of Tertiary Difluoroketones via Weinreb Amide Homologation with a CHF2-Carbene Equivalent

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