Issue 39, 2015

Total syntheses of natural products containing spirocarbocycles

Abstract

The structures of natural products from a variety of sources contain spirocycles, two rings that share a common atom. The spiro motif is finding increasing inclusion in drug candidates, and as a structural component in several promising classes of chiral ligands used in asymmetric synthesis. Total syntheses of products containing all-carbon spirocycles feature several common methods of ring closure which we examine in this review.

Graphical abstract: Total syntheses of natural products containing spirocarbocycles

Article information

Article type
Review Article
Submitted
23 Jul 2015
Accepted
01 Sep 2015
First published
01 Sep 2015
This article is Open Access
Creative Commons BY license

Org. Biomol. Chem., 2015,13, 9907-9933

Author version available

Total syntheses of natural products containing spirocarbocycles

L. K. Smith and I. R. Baxendale, Org. Biomol. Chem., 2015, 13, 9907 DOI: 10.1039/C5OB01524C

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