Issue 49, 2015

Regioselectivity switch in chiral amine-catalysed asymmetric addition of aldehydes to reactive enals

Abstract

In this communication, we present a regioselectivity switch for the chiral amine-catalysed asymmetric addition of aldehydes to reactive enals to afford either aldol adducts or conjugate adducts in a stereoselective fashion. The unprecedented asymmetric aldol reaction of aldehydes with enals was realized by the use of a diarylprolinol catalyst, giving synthetically useful and important chiral allylic alcohols.

Graphical abstract: Regioselectivity switch in chiral amine-catalysed asymmetric addition of aldehydes to reactive enals

Supplementary files

Article information

Article type
Communication
Submitted
22 Apr 2015
Accepted
12 May 2015
First published
12 May 2015

Chem. Commun., 2015,51, 10062-10065

Author version available

Regioselectivity switch in chiral amine-catalysed asymmetric addition of aldehydes to reactive enals

T. Kano, H. Maruyama, R. Sakamoto and K. Maruoka, Chem. Commun., 2015, 51, 10062 DOI: 10.1039/C5CC02438B

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