Enantioselective synthesis of (S)-salmeterol via asymmetric reduction of azidoketone by Pichia angusta

Authors
Procopiou, PA Morton, GE Todd, M Webb, G
Citation
Pa. Procopiou et al., Enantioselective synthesis of (S)-salmeterol via asymmetric reduction of azidoketone by Pichia angusta, TETRAHEDR-A, 12(14), 2001, pp. 2005-2008
Citations number
10
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON-ASYMMETRY
ISSN journal
09574166 → ACNP
Volume
12
Issue
14
Year of publication
2001
Pages
2005 - 2008
Database
ISI
SICI code
0957-4166(20010814)12:14<2005:ESO(VA>2.0.ZU;2-I
Abstract
An efficient enantioselective route to (S)-salmeterol involving asymmetric reduction of an azidoketone intermediate to an azido alcohol by Pichia angu sta is described. (C) 2001 Elsevier Science Ltd. All rights reserved.