Issue 26, 2007

Indium–bipyridine-catalyzed, enantioselective thiolysis of meso-epoxides

Abstract

The indium–bipyridine-catalyzed, enantioselective ring-opening of meso-epoxides with aliphatic and aromatic thiols furnished 1,2-mercapto alcohols in good yields and excellent enantioselectivities; the crystal structure of the chiral catalyst reveals a pentagonal-bipyramidal coordination geometry around the indium center.

Graphical abstract: Indium–bipyridine-catalyzed, enantioselective thiolysis of meso-epoxides

Supplementary files

Article information

Article type
Communication
Submitted
12 Mar 2007
Accepted
03 Apr 2007
First published
24 Apr 2007

Chem. Commun., 2007, 2756-2758

Indium–bipyridine-catalyzed, enantioselective thiolysis of meso-epoxides

M. V. Nandakumar, A. Tschöp, H. Krautscheid and C. Schneider, Chem. Commun., 2007, 2756 DOI: 10.1039/B703625F

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