Issue 39, 2016

A switchable dual organocatalytic system and the enantioselective total synthesis of the quadrane sesquiterpene suberosanone

Abstract

The combination of aminocatalysis with N-heterocyclic carbene catalysis has been extended to a switchable dual catalytic system, which allowed a direct enantioselective entry to bridged bicyclo[3.n.1] ring systems and the total synthesis of the natural product (1R)-suberosanone.

Graphical abstract: A switchable dual organocatalytic system and the enantioselective total synthesis of the quadrane sesquiterpene suberosanone

Supplementary files

Article information

Article type
Communication
Submitted
24 Feb 2016
Accepted
15 Apr 2016
First published
15 Apr 2016
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2016,52, 6565-6568

A switchable dual organocatalytic system and the enantioselective total synthesis of the quadrane sesquiterpene suberosanone

Y. Ren, M. Presset, J. Godemert, N. Vanthuyne, J. Naubron, M. Giorgi, J. Rodriguez and Y. Coquerel, Chem. Commun., 2016, 52, 6565 DOI: 10.1039/C6CC01689H

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, 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 commercial 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