Asymmetric reduction of prochiral ketones using in situ generated oxazaborolidines derived from amino alcohols of (1R)-camphor as catalysts

Authors
Santhi, V Rao, JM
Citation
V. Santhi et Jm. Rao, Asymmetric reduction of prochiral ketones using in situ generated oxazaborolidines derived from amino alcohols of (1R)-camphor as catalysts, TETRAHEDR-A, 11(17), 2000, pp. 3553-3560
Citations number
17
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON-ASYMMETRY
ISSN journal
09574166 → ACNP
Volume
11
Issue
17
Year of publication
2000
Pages
3553 - 3560
Database
ISI
SICI code
0957-4166(20000908)11:17<3553:AROPKU>2.0.ZU;2-6
Abstract
Chiral oxazaborolidines generated in situ from 1,2-amino alcohols and amino alcohol derivatives derived from (1R)-(+)-camphor and borane or trimethyl berate were used as catalysts for the enantioselective reduction of prochir al ketones. (C) 2000 Published by Elsevier Science Ltd.