Chiral Covalent Organic Frameworks: An emerging standalone photocatalyst for asymmetric organic transformations

Abstract

Synthetic chemists continue to face significant challenges in synthesis of organic molecules with precise control over absolute stereochemistry. In this review, we cover recent advances in enantioselective transformations enabled by chiral covalent organic frameworks (CCOFs) as standalone photocatalysts. These CCOFs integrate a photoactive unit and a chiral element into a single platform, in which, the photocatalytic component activates the substrates, while the chiral component directs stereo induction. Although researchers have so far limited synthetic applications to a small set of benchmark C-C bond formations and oxidation processes, the scope of these transformations is expected to expand steadily in the near future. Inter-disciplinary knowledge transfer from asymmetric catalysis is driving this growth and is also enabling the extension of these materials into broader applications, including chiral separations, asymmetric electrocatalysis for organic synthesis and chiral sensing technologies.

Transparent peer review

To support increased transparency, we offer authors the option to publish the peer review history alongside their article.

View this article’s peer review history

Article information

Article type
Review Article
Submitted
27 Mar 2026
Accepted
23 Apr 2026
First published
24 Apr 2026
This article is Open Access
Creative Commons BY license

Chem. Commun., 2026, Accepted Manuscript

Chiral Covalent Organic Frameworks: An emerging standalone photocatalyst for asymmetric organic transformations

A. Das, A. H. Ibrahim and V. Kumar S, Chem. Commun., 2026, Accepted Manuscript , DOI: 10.1039/D6CC01863G

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements