Visible-light-induced organocatalytic enantioselective N–H insertion of α-diazoesters enabled by indirect free carbene capture

Author:

Guo Wengang1ORCID,Zhou Ying1,Xie Hongling1,Yue Xin1,Jiang Feng1,Huang Hai1ORCID,Han Zhengyu1,Sun Jianwei123ORCID

Affiliation:

1. Advanced Catalysis and Green Manufacturing Collaborative Innovation Center, School of Petrochemical Engineering, Changzhou University, Changzhou, 213164, China

2. Department of Chemistry, The Hong Kong Branch of Chinese National Engineering Research Centre for Tissue Restoration & Reconstruction, The Hong Kong University of Science and Technology (HKUST), Clear Water Bay, Kowloon, Hong Kong SAR, China

3. Shenzhen Research Institute, HKUST, No. 9 Yuexing 1st Rd, Shenzhen 518057, China

Abstract

It has been a long-standing challenge to achieve catalytic asymmetric X–H bond insertion with free carbenes. Herein, an indirect visible-light-promoted asymmetric N–H insertion is disclosed.

Funder

Research Grants Council, University Grants Committee

Innovation and Technology Commission

Changzhou University

Jiangsu Key Laboratory of Advanced Catalytic Materials and Technology Department

Science, Technology and Innovation Commission of Shenzhen Municipality

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemistry

Reference70 articles.

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3. J.March , Advanced Organic Chemistry: Reactions, Mechanisms, and Structure , Wiley-Interscience , New York , 6th edn, 2007

4. Catalytic Enantioselective C−H Activation by Means of Metal−Carbenoid-Induced C−H Insertion

5. Catalytic Carbene Insertion into C−H Bonds

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