A simple method for N-arylation of secondary amides/amines through a NaH-initiated aryne generation strategy

Author:

Jiang Yuanrui1,Zhu Wenjing1,Huang Jiawen1,Luo Fan2,Chen Xiaobei3,Fang Chunhui1,Chen Xin1,Liu Shihui2ORCID,Hu Yanwei1,Zhang Shilei1ORCID

Affiliation:

1. Jiangsu Key Laboratory of Neuropsychiatric Diseases and College of Pharmaceutical Sciences, Soochow University, 199 Ren'ai Road, Suzhou, Jiangsu, 215123, P. R. China

2. College of Medicine, Jiaxing University, 118 Jiahang Road, Jiaxing 314001, P. R. China

3. Shanghai Frontiers Science Center of Optogenetic Techniques for Cell Metabolism, Shanghai Key Laboratory of New Drug Design, and State Key Laboratory of Bioreactor Engineering, School of Pharmacy, East China University of Science & Technology, Shanghai, 200237, P. R. China

Abstract

A very simple and practical method has been uncovered for N-arylation of many sets of secondary amides/amines.

Funder

National Natural Science Foundation of China

East China University of Science and Technology

Priority Academic Program Development of Jiangsu Higher Education Institutions

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

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