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

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 ar...

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Veröffentlicht in:Chemical communications (Cambridge, England) England), 2007-01 (26), p.2756-2758
Hauptverfasser: Nandakumar, Mecheril Valsan, Tschöp, Andreas, Krautscheid, Harald, Schneider, Christoph
Format: Artikel
Sprache:eng
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Zusammenfassung: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.
ISSN:1359-7345
1364-548X
DOI:10.1039/b703625f