Issue 2, 2023

Deaminative defluoroalkylation of α-trifluoromethylalkenes enabled by photoredox catalysis

Abstract

Herein, we disclose a new photoredox-catalysed strategy to access gem-difluoroallylarenes from α-trifluoromethylalkenes with sterically hindered primary amines via C–N and C–F bond activation. This deaminative and defluorinative allylation is generally compatible with diverse functional groups and sterically hindered α-3° and 2° primary amines.

Graphical abstract: Deaminative defluoroalkylation of α-trifluoromethylalkenes enabled by photoredox catalysis

Supplementary files

Article information

Article type
Communication
Submitted
21 Nov 2022
Accepted
02 Dec 2022
First published
05 Dec 2022

Org. Biomol. Chem., 2023,21, 294-299

Deaminative defluoroalkylation of α-trifluoromethylalkenes enabled by photoredox catalysis

G. Zhang, L. Wang, L. Cui, P. Gao and F. Chen, Org. Biomol. Chem., 2023, 21, 294 DOI: 10.1039/D2OB02114E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements