Issue 21, 1991

The orthoester Claisen rearrangement in the synthesis of mycophenolic acid

Abstract

The orthoester Claisen rearrangement is used as a key reaction in the facile conversion of an acetaldehyde moiety stereospecifically into the (E)-4-methylhex-4-enoic acid side-chain of mycophenolic acid.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1991, 1579-1580

The orthoester Claisen rearrangement in the synthesis of mycophenolic acid

J. W. Patterson and G. T. Huang, J. Chem. Soc., Chem. Commun., 1991, 1579 DOI: 10.1039/C39910001579

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.

Spotlight

Advertisements