Issue 8, 2010

Stereoselective transition metal-catalysed higher-order carbocyclisation reactions

Abstract

Transition metal-catalysed higher-order carbocyclisation reactions represent an important class of reactions due to their ability to construct complex polycyclic systems in a highly selective and atom-economical fashion. A key and striking feature with these transformations is the dichotomy in reactivity that a substrate displays with different transition metal complexes, which is akin to the manner enzymes direct terpene biosynthesis. This tutorial review details the historical development of higher-order carbocyclisation reactions, specifically the variants of [m+2+2] that involve carbon-based π-systems, where m = 2, 3 and 4, in the context of critical developments with various transition metal complexes.

Graphical abstract: Stereoselective transition metal-catalysed higher-order carbocyclisation reactions

Article information

Article type
Tutorial Review
Submitted
25 Jan 2010
First published
27 May 2010

Chem. Soc. Rev., 2010,39, 2791-2805

Stereoselective transition metal-catalysed higher-order carbocyclisation reactions

P. A. Inglesby and P. A. Evans, Chem. Soc. Rev., 2010, 39, 2791 DOI: 10.1039/B913110H

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