Issue 21, 2023

β-Trifluoromethylated enones as trifluoromethylated synthons in asymmetric catalysis

Abstract

Trifluoromethylated organic molecules are ubiquitous in pharmaceutics, materials science, and agrochemicals. In the past few decades, great efforts have been devoted to the development of convenient and efficient strategies for the synthesis of these compounds. β-Trifluoromethylated enones are readily available building blocks, and are recognized as an attractive synthetic feedstock in organic transformations. Thus far, numerous new catalytic systems including novel chiral ligands and organocatalysts have been applied to asymmetric catalytic protocols using β-trifluoromethylated enones and various optically active compounds containing CF3 motif have been synthesized. Hence, this minireview describes the applications of β-trifluoromethylated enones in diverse asymmetric catalytic transformations since 2008, and incorporates the mechanistic aspects, involving the key mechanistic intermediates and the reaction pathways. Finally, the challenges of related fields and future perspectives are also pointed out.

Graphical abstract: β-Trifluoromethylated enones as trifluoromethylated synthons in asymmetric catalysis

Article information

Article type
Review Article
Submitted
23 avq 2023
Accepted
19 sen 2023
First published
20 sen 2023

Org. Chem. Front., 2023,10, 5519-5537

β-Trifluoromethylated enones as trifluoromethylated synthons in asymmetric catalysis

X. Cheng, W. Niu, H. Wang and Y. Lin, Org. Chem. Front., 2023, 10, 5519 DOI: 10.1039/D3QO01357J

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