Issue 7, 1996

Unexpected asymmetric epoxidation reactions catalysed by polyleucine-based systems

Abstract

Polyleucine-based systems have been shown to catalyse the asymmetric epoxidation of a variety of enones, an enynone, selected enediones and an unsaturated ketoster.

Article information

Article type
Paper

Chem. Commun., 1996, 845-846

Unexpected asymmetric epoxidation reactions catalysed by polyleucine-based systems

W. Kroutil, P. Mayon, M. E. Lasterra-Sánchez, S. J. Maddrell, S. M. Roberts, S. R. Thornton, C. J. Todd and M. Tüter, Chem. Commun., 1996, 845 DOI: 10.1039/CC9960000845

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