Jump to main content
Jump to site search

Issue 18, 2012

Enantioselective total synthesis of (+)-galbulinvia organocatalytic domino Michael–Michael–aldol condensation

Author affiliations

Abstract

A concise and practical enantioselective synthesis of (+)-galbulin has been achieved using organocatalytic domino Michael–Michael–aldol condensation and organocatalytic kinetic resolution as the key steps.

Graphical abstract: Enantioselective total synthesis of (+)-galbulinvia organocatalytic domino Michael–Michael–aldol condensation

Supplementary files

Article information


Submitted
28 Oct 2011
Accepted
29 Nov 2011
First published
01 Dec 2011

Chem. Commun., 2012,48, 2385-2387
Article type
Communication

Enantioselective total synthesis of (+)-galbulinvia organocatalytic domino Michael–Michael–aldol condensation

B. Hong, C. Hsu and G. Lee, Chem. Commun., 2012, 48, 2385 DOI: 10.1039/C2CC16682H

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

Search articles by author

Spotlight

Advertisements