Issue 22, 2017

Aerobic catalytic systems inspired by copper amine oxidases: recent developments and synthetic applications

Abstract

Recent efforts to design synthetic quinone-based catalysts for the efficient aerobic oxidation of amines to imines have been inspired by copper amine oxidases (CuAOs), a family of metalloenzymes which selectively converts primary amines into aldehydes, using molecular oxygen through the cooperation of a quinone-based cofactor, 2,4,5-trihydroxyphenylalanine quinone (TPQ) and a copper ion. Two distinct classes of bioinspired quinone-based catalytic systems have been developed. The first class consists of catalytic systems, which mimic the activity of CuAOs by exhibiting exquisite selectivity for primary amines. The second class consists of catalytic systems, which allow the expansion of the substrate scope to the oxidation of α-branched primary amines and secondary amines including nitrogen heterocycles, two reaction types that natural CuAOs are not able to accomplish. These catalytic oxidative green processes can be applied to the C–H functionalization of primary amines and to the synthesis of several nitrogen-containing heterocycles.

Graphical abstract: Aerobic catalytic systems inspired by copper amine oxidases: recent developments and synthetic applications

Article information

Article type
Review Article
Submitted
28 Yan 2017
Accepted
25 Dzi 2017
First published
25 Dzi 2017

Org. Biomol. Chem., 2017,15, 4722-4730

Aerobic catalytic systems inspired by copper amine oxidases: recent developments and synthetic applications

M. Largeron, Org. Biomol. Chem., 2017, 15, 4722 DOI: 10.1039/C7OB00507E

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