Unprecedented single-electron-transfer reduction-based N → C acyl migration reactions of imides enabled by redox-neutral photocatalysis-Reference-Cited by-同舟云学术

Unprecedented single-electron-transfer reduction-based N → C acyl migration reactions of imides enabled by redox-neutral photocatalysis

Published:2024 Issue:8 Volume:11 Page:2344-2350
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Huai Linge¹,Zhang Li²,Wang Zhentao¹,Fang Yewen³⁴^ORCID

Affiliation:

1. College of Chemistry and Material Science, Shandong Agricultural University, No. 61 Daizong Road, Tai'an 271018, China

2. School of Fundamental Science, Zhejiang Pharmaceutical University, No. 666 Siming Road, Ningbo 315500, China

3. School of Materials and Chemical Engineering, Ningbo University of Technology, No. 201 Fenghua Road, Ningbo 315211, China

4. Zhejiang Institute of Tianjin University, No. 201 Fenghua Road, Ningbo 315211, China

Abstract

N → C acyl migration: in the absence of a base, redox-neutral photocatalyzed acyl migration reactions have been realized via the reaction of N-vinylimides with alkyl radicals derived from alkyl silicates.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Ningbo

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D3QO01955A

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