Jump to main content
Jump to site search


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

Author affiliations

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

Back to tab navigation

Supplementary files

Article information


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

Org. Biomol. Chem., 2020, Advance Article
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, Advance Article , DOI: 10.1039/C9OB02600B

Social activity

Search articles by author

Spotlight

Advertisements