Issue 60, 2023

H2O2-driven enzymatic oxyfunctionalization of tertiary C–H bonds

Abstract

Peroxygenase from Agrocybe aegerita catalyses the selective hydroxylation of tertiary C–H bonds, whereby tertiary alcohols, diols, ketols, etc., were obtained in good to high regioselectivity and turnover numbers. This method can also be expanded for late-stage functionalization of drug molecules, which represents a streamlined synthetic method to give access to useful compounds.

Graphical abstract: H2O2-driven enzymatic oxyfunctionalization of tertiary C–H bonds

Supplementary files

Article information

Article type
Communication
Submitted
19 Jun 2023
Accepted
03 Jul 2023
First published
03 Jul 2023

Chem. Commun., 2023,59, 9219-9222

H2O2-driven enzymatic oxyfunctionalization of tertiary C–H bonds

Y. Huang, H. Li, P. Zhang, Y. Zhang, P. Duan and W. Zhang, Chem. Commun., 2023, 59, 9219 DOI: 10.1039/D3CC02925E

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