Volume 43, Issue 2 pp. 155-160
Concise Report

Catalyst-Free, Radical Tri- and Difluoromethylation of Isocyanides and N-Arylacrylamides Using Rotating Magnetic Field and Metal Rods

Xuliang Han

Xuliang Han

School of Chemistry and Chemical Engineering, Shandong University of Technology, Zibo, Shandong, 255000 China

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Haodong Liu

Haodong Liu

School of Chemistry and Chemical Engineering, Shandong University of Technology, Zibo, Shandong, 255000 China

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Xiaomei Feng

Xiaomei Feng

School of Chemistry and Chemical Engineering, Shandong University of Technology, Zibo, Shandong, 255000 China

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Fuchao Jia

Fuchao Jia

School of Physics and Optoelelctronic Engineering, Shandong University of Technology, Zibo, Shandong, 255000 China

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Zengdian Zhao

Zengdian Zhao

School of Chemistry and Chemical Engineering, Shandong University of Technology, Zibo, Shandong, 255000 China

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Xinjin Li

Corresponding Author

Xinjin Li

School of Chemistry and Chemical Engineering, Shandong University of Technology, Zibo, Shandong, 255000 China

E-mail: [email protected]Search for more papers by this author
First published: 07 October 2024
Citations: 5

Comprehensive Summary

The pursuit of sustainable and environmentally benign synthetic methods continues to challenge organic chemists. Herein, we introduce a magnetoredox system for tri- and difluoromethylation of isocyanides and N-arylacrylamides using a rotating magnetic field and steel rods. This magnetoredox approach enables facile synthesis of functionalized phenanthridines and oxindoles without the need for catalysts and additives under mild conditions. Such a system potentially represents an attractive strategy for selective formation of bonds through multifaceted regulation of magnetic intensity, rotating frequency, and rod size.

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