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Issue 5, 2020

Visible-light-promoted radical cross-coupling of para-quinone methides with N-substituted anilines: an efficient approach to 2,2-diarylethylamines

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Abstract

An efficient protocol to access 2,2-diarylethylamines via visible-light-promoted radical reactions of para-quinone methides (p-QMs) with N-alkyl anilines has been disclosed. These reactions feature metal-free, redox-neutral, and mild reaction conditions with wide functional group compatibility.

Graphical abstract: Visible-light-promoted radical cross-coupling of para-quinone methides with N-substituted anilines: an efficient approach to 2,2-diarylethylamines

Supplementary files

Article information


Submitted
06 Dec 2019
Accepted
11 Jan 2020
First published
13 Jan 2020

Org. Biomol. Chem., 2020,18, 860-864
Article type
Communication

Visible-light-promoted radical cross-coupling of para-quinone methides with N-substituted anilines: an efficient approach to 2,2-diarylethylamines

Q. Wu, J. Guo, G. Huang, A. S. C. Chan, J. Weng and G. Lu, Org. Biomol. Chem., 2020, 18, 860 DOI: 10.1039/C9OB02600B

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