Issue 7, 2009

Recyclable organocatalysis: highly enantioselective Michael addition of 1,3-diaryl-1,3-propanedione to nitroolefins

Abstract

The first Michael addition of 1,3-diaryl-1,3-propanedione to nitroolefins was demonstrated using a simple organocatalyst, which afforded excellent yields (81–97%) and enantioselectivities (90 to >99% ee); the catalyst and excess reactant can be reused seven times through a simple filtration operation.

Graphical abstract: Recyclable organocatalysis: highly enantioselective Michael addition of 1,3-diaryl-1,3-propanedione to nitroolefins

Supplementary files

Article information

Article type
Communication
Submitted
12 Aug 2008
Accepted
31 Oct 2008
First published
20 Nov 2008

Chem. Commun., 2009, 779-781

Recyclable organocatalysis: highly enantioselective Michael addition of 1,3-diaryl-1,3-propanedione to nitroolefins

B. Tan, X. Zhang, P. J. Chua and G. Zhong, Chem. Commun., 2009, 779 DOI: 10.1039/B813915F

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