Issue 3, 2010

Biosynthesis of ethers: Unusual or common natural events?

Abstract

Covering: up to the end of 2007

Ether bonds are found in a wide variety of natural products – mainly secondary metabolites – including lipids, oxiranes, terpenoids, flavonoids, polyketides, and carbohydrate derivatives, to name some representative examples. To furnish such a biodiversity of structures, a large number of different enzymes are involved in several different biosynthetic pathways. Depending on the compound and on the (micro)environment in which the reaction is performed, ethers are produced by very different (enzymatic) reactions, thus providing an impressive display of how Nature has combined evolution and thermodynamics to be able to produce a vast number of compounds. In addition, many of these compounds possess different biological activities of pharmacological interest. Moreover, some of these ethers (i.e., epoxides) have high chemical reactivity, and can be useful starting materials for further synthetic processes. This review aims to provide an overview of the different strategies that are found in Nature for the formation of these ‘bioethers’. Both fundamental and practical insights of the biosynthetic processes will be discussed.

Graphical abstract: Biosynthesis of ethers: Unusual or common natural events?

Article information

Article type
Review Article
Submitted
05 Oct 2009
First published
02 Feb 2010

Nat. Prod. Rep., 2010,27, 370-392

Biosynthesis of ethers: Unusual or common natural events?

P. Domínguez de María, R. W. van Gemert, A. J. J. Straathof and U. Hanefeld, Nat. Prod. Rep., 2010, 27, 370 DOI: 10.1039/B809416K

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