Issue 8, 2022

Recent advances in the catalytic asymmetric construction of atropisomers by central-to-axial chirality transfer

Abstract

Atropisomeric compounds, referring to the compounds showing restricted rotation of a single bond, have recently received much attention as an important class of chiral molecules. Their significance is not only derived from their use as catalysts and ligands in asymmetric synthesis, but also due to their presence in many common scaffolds in drug discovery and natural products including axially chiral biaryls, arylamides and anilides. Thus, an increasing number of catalytic methods have been developed for their direct asymmetric preparation. In this context, central-to-axial chirality transfer serves as a promising strategy that has been widely used for constructing many atropisomeric compounds. This review, herein, highlights the recent advances (from 2010 to 2021) in the stereoselective synthesis of atropisomers by central-to-axial chirality transfer.

Graphical abstract: Recent advances in the catalytic asymmetric construction of atropisomers by central-to-axial chirality transfer

Article information

Article type
Review Article
Submitted
13 Nov 2021
Accepted
25 Feb 2022
First published
10 Mar 2022

Org. Chem. Front., 2022,9, 2280-2292

Recent advances in the catalytic asymmetric construction of atropisomers by central-to-axial chirality transfer

X. Min, X. Zhang, R. Shen, Q. Zhang and Y. He, Org. Chem. Front., 2022, 9, 2280 DOI: 10.1039/D1QO01699G

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