Issue 18, 2014

Catalytic asymmetric conjugate addition of terminal alkynes to β-trifluoromethyl α,β-enones

Abstract

The first enantioselective conjugate alkynylation of β-trifluoromethyl α,β-enones using terminal alkynes and a taniaphos–Cu(I) complex as catalyst is described. Ketones bearing a trifluoromethylated propargylic chiral centre in the β-position were obtained with good yields and high enantiomeric excesses (up to 99%).

Graphical abstract: Catalytic asymmetric conjugate addition of terminal alkynes to β-trifluoromethyl α,β-enones

Supplementary files

Article information

Article type
Communication
Submitted
07 Nov 2013
Accepted
27 Dec 2013
First published
06 Jan 2014

Chem. Commun., 2014,50, 2275-2278

Author version available

Catalytic asymmetric conjugate addition of terminal alkynes to β-trifluoromethyl α,β-enones

A. Sanz-Marco, A. García-Ortiz, G. Blay and J. R. Pedro, Chem. Commun., 2014, 50, 2275 DOI: 10.1039/C3CC48508K

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