Catalytic Asymmetric Reactions of Indolylmethanols for the Synthesis of Chiral Indole Derivatives

Abstract

Owing to the importance of chiral indole derivatives, catalytic asymmetric transformations of indole-based platform molecules have proven to be robust methods toward the enantioselective synthesis of such compounds. Particularly, indolylmethanols serve as versatile indole-based platform molecules for catalytic asymmetric construction of chiral indole scaffolds. As a result, significant progress has been made in the field of catalytic asymmetric reactions of indolylmethanols. This feature article reviews the latest advances in catalytic asymmetric reactions of indolylmethanols, including those from our group, by giving representative examples and insightful analysis. Moreover, the remaining issues in this field are pointed out, which will inspire chemists to devise new class of indolylmethanol platform molecules, innovative catalytic strategies and asymmetric transformations, thus promoting the further development of chiral indole chemistry.

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
Feature Article
Submitted
23 Oct 2025
Accepted
27 Nov 2025
First published
28 Nov 2025

Chem. Commun., 2025, Accepted Manuscript

Catalytic Asymmetric Reactions of Indolylmethanols for the Synthesis of Chiral Indole Derivatives

Y. Wang, W. Luan, C. Ma and F. Shi, Chem. Commun., 2025, Accepted Manuscript , DOI: 10.1039/D5CC06044C

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