Issue 34, 2014

Enantio- and chemoselective Brønsted-acid/Mg(nBu)2 catalysed reduction of α-keto esters with catecholborane

Abstract

The first enantio- and chemoselective Brønsted-acid catalysed reduction of α-keto esters with catecholborane has been developed. The α-hydroxy esters were obtained under mild reaction conditions in virtually quantitative yields and excellent enantioselectivities. With slight modifications both enantiomers can be obtained without any loss of selectivity.

Graphical abstract: Enantio- and chemoselective Brønsted-acid/Mg(nBu)2 catalysed reduction of α-keto esters with catecholborane

Supplementary files

Article information

Article type
Communication
Submitted
17 Jan 2014
Accepted
04 Mar 2014
First published
05 Mar 2014

Chem. Commun., 2014,50, 4489-4491

Author version available

Enantio- and chemoselective Brønsted-acid/Mg(nBu)2 catalysed reduction of α-keto esters with catecholborane

D. Enders, B. A. Stöckel and A. Rembiak, Chem. Commun., 2014, 50, 4489 DOI: 10.1039/C4CC00427B

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