SCHEDULED MAINTENANCE
Enantioselective route to (–)-chokol A
Abstract
Stereoselective introduction of a methyl group to (3R)-2-methylcyclopentanone (2), followed by orthoester Claisen rearrangement provided the methyl ester (6) leading to (–)-chokol A (4).
Please wait while we load your content...
Article information
- Article type
- Paper
J. Chem. Soc., Chem. Commun., 1988, 1531-1533
Permissions
Enantioselective route to (–)-chokol A
T. Suzuki, E. Sato, Y. Matsuda, H. Tada, S. Koizumi, K. Unno and T. Kametani, J. Chem. Soc., Chem. Commun., 1988, 1531 DOI: 10.1039/C39880001531
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.