Issue 1, 1999

Asymmetric Claisen rearrangement

Abstract

Development of the asymmetric Claisen rearrangement is one of the challenging tasks in synthetic organic chemistry. There have been numerous reports of the asymmetric Claisen rearrangement based on the intramolecular chirality transfer using chiral substrates. On the other hand, reactions of achiral substrates with an external chiral activator have been studied during the last decade. In this review article, recent advances in the asymmetric Claisen rearrangement are described.

Article information

Article type
Paper

Chem. Soc. Rev., 1999,28, 43-50

Asymmetric Claisen rearrangement

H. Ito and T. Taguchi, Chem. Soc. Rev., 1999, 28, 43 DOI: 10.1039/A706415B

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