Issue 40, 2021

Recent advances in intermolecular 1,2-difunctionalization of alkenes involving trifluoromethylthiolation

Abstract

Trifluoromethylthiolative difunctionalization of alkenes, a cheap and abundant feedstock, which installs a trifluoromethylthiol (SCF3) group and another unique functional group across the carbon–carbon double bonds, provides an ideal strategy for the preparation of β-functionalized alkyl trifluoromethyl sulfides and has become a hot topic recently. This review aims to summarize the major progress in this exciting research area, with particular emphasis on the mechanistic aspects of the reaction pathways.

Graphical abstract: Recent advances in intermolecular 1,2-difunctionalization of alkenes involving trifluoromethylthiolation

Article information

Article type
Review Article
Submitted
02 Apr 2021
Accepted
17 Jun 2021
First published
13 Jul 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 24474-24486

Recent advances in intermolecular 1,2-difunctionalization of alkenes involving trifluoromethylthiolation

L. Yan-mei, F. Jin-feng, H. Long-qiang, L. Wei-na and E. Vessally, RSC Adv., 2021, 11, 24474 DOI: 10.1039/D1RA02606B

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, 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 commercial 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