Issue 11, 2009

Application of donor/acceptor-carbenoids to the synthesis of natural products

Abstract

The metal catalyzed reactions of diazo compounds have been broadly used in organic synthesis. The resulting metal–carbenoid intermediates are capable of undergoing a range of unconventional reactions, and due to their high energy, they are ideal for initiating cascade sequences leading to the rapid generation of structural complexity. This tutorial review will give an overview of the most versatile reactions of donor/acceptor carbenoids, an exciting class of intermediates capable of highly selective reactions. This will include cyclopropanation, [4 + 3] cycloaddition, and C–H functionalization methodologies. The application of this chemistry to the synthesis of a range of natural products will be described.

Graphical abstract: Application of donor/acceptor-carbenoids to the synthesis of natural products

Article information

Article type
Tutorial Review
Submitted
09 Jul 2009
First published
30 Sep 2009

Chem. Soc. Rev., 2009,38, 3061-3071

Application of donor/acceptor-carbenoids to the synthesis of natural products

H. M. L. Davies and J. R. Denton, Chem. Soc. Rev., 2009, 38, 3061 DOI: 10.1039/B901170F

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