Issue 25, 2017

Enantioselective Barbier-type allylation of ketones using allyl halide and indium in water

Abstract

We disclose herein an efficient enantioselective Barbier-type allylation of ketones using allyl halide and indium metal in water. The reaction was catalysed by chiral bis(imidazoline) to afford homoallylic alcohols having quaternary stereocenters in good yield with moderate to good enantioselectivity. Based on experimental investigation, a possible transition state has been proposed to explain the origin of the asymmetric induction.

Graphical abstract: Enantioselective Barbier-type allylation of ketones using allyl halide and indium in water

Supplementary files

Article information

Article type
Paper
Submitted
23 Jan 2017
Accepted
03 Mar 2017
First published
09 Mar 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 15582-15585

Enantioselective Barbier-type allylation of ketones using allyl halide and indium in water

S. Nakamura, Y. Hara, T. Furukawa and T. Hirashita, RSC Adv., 2017, 7, 15582 DOI: 10.1039/C7RA01038A

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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