Cyclopropanation ofN-vinylimidesviaa redox-neutral photocatalysed radical addition/anionic cyclisation process

Author:

Huai Linge1,Zhang Li2,Wang Zhentao1,Wu Hao3,Fang Yewen34ORCID

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

Cyclopropylamine synthesis: using halomethyl radicals as the CH2source, photoredox-catalysed cyclopropanation ofN-vinylimides could proceed well, giving modular access to 1- or 2-arylcyclopropylamines.

Funder

National Natural Science Foundation of China

Ningbo Natural Science Foundation

Science and Technology Innovation 2025 Major Project of Ningbo

Department of Education of Zhejiang Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

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