Issue 27, 2019

Catalytic enantioselective Hosomi–Sakurai reaction of α-ketoesters promoted by chiral copper(ii) complexes

Abstract

A catalytic enantioselective Hosomi–Sakurai reaction of α-ketoesters has been developed. A copper(II) complex with a chiral bis(oxazoline) ligand bearing methanesulfonamide groups shows excellent catalytic activity to give α,α-disubstituted α-hydroxyesters in high yields with high enantioselectivities. This is the first successful method for the catalytic enantioselective 1,2-addition of α-ketoesters with allylic silanes.

Graphical abstract: Catalytic enantioselective Hosomi–Sakurai reaction of α-ketoesters promoted by chiral copper(ii) complexes

Supplementary files

Article information

Article type
Communication
Submitted
09 Feb 2019
Accepted
05 Mar 2019
First published
05 Mar 2019

Chem. Commun., 2019,55, 3923-3926

Catalytic enantioselective Hosomi–Sakurai reaction of α-ketoesters promoted by chiral copper(II) complexes

Y. Niwa, M. Miyake, I. Hayakawa and A. Sakakura, Chem. Commun., 2019, 55, 3923 DOI: 10.1039/C9CC01159E

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