Issue 47, 2019

Recent advances in direct trifluoromethylation of olefinic C–H bonds

Abstract

The aim of this review is to provide a comprehensive overview of the direct trifluoromethylation of olefinic C–H bonds with special attention on the mechanistic aspects of the reactions. The review is divided into two major sections. The first focuses exclusively on trifluoromethylation of terminal alkenes, while the second will cover trifluoromethylation of internal alkenes. Literature has been surveyed until the end of April 2019.

Graphical abstract: Recent advances in direct trifluoromethylation of olefinic C–H bonds

Article information

Article type
Review Article
Submitted
02 Jun 2019
Accepted
21 Aug 2019
First published
03 Sep 2019
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2019,9, 27625-27639

Recent advances in direct trifluoromethylation of olefinic C–H bonds

C. Yang, A. Hassanpour, K. Ghorbanpour, S. Abdolmohammadi and E. Vessally, RSC Adv., 2019, 9, 27625 DOI: 10.1039/C9RA04170B

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