SYNTHESIS OF ENANTIOMERICALLY PURE (1S,2R)-EPOXY INDANE AND CIS-(1R,2S)-2-AMINO-1-INDANOL

Authors
MITROCHKINE A EYDOUX F MARTRES M GIL G HEUMANN A REGLIER M
Citation
A. Mitrochkine et al., SYNTHESIS OF ENANTIOMERICALLY PURE (1S,2R)-EPOXY INDANE AND CIS-(1R,2S)-2-AMINO-1-INDANOL, Tetrahedron : asymmetry, 6(1), 1995, pp. 59-62
Citations number
15
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear","Chemistry Physical
Journal title
Tetrahedron : asymmetry → ACNP
ISSN journal
09574166
Volume
6
Issue
1
Year of publication
1995
Pages
59 - 62
Database
ISI
SICI code
0957-4166(1995)6:1<59:SOEP(I>2.0.ZU;2-2
Abstract
Enantiomerically pure (1S, 2R)-epoxy indane and cis-(1R, 2S)-2-amino-1 -indanol were synthesized via highly enantioselective lipase catalyzed transesterification of racemic trans-2-bromo-1-indanol.