Catalytic activation of trichlorosilane for efficient and stereoselective reduction of ketones

Citation
F. Iwasaki et al., Catalytic activation of trichlorosilane for efficient and stereoselective reduction of ketones, TETRAHEDR L, 40(42), 1999, pp. 7507-7511
Citations number
14
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
40
Issue
42
Year of publication
1999
Pages
7507 - 7511
Database
ISI
SICI code
0040-4039(19991015)40:42<7507:CAOTFE>2.0.ZU;2-G
Abstract
Some kinds of N-formyl cyclic amine derivatives were found to be effective activators for trichlorosilane to reduce ketones. Namely, a catalytic amoun t of these activators were sufficient to complete the reduction of ketones with trichlorosilane, and the reduction of ketones by trichlorosilane with optically active activators gave enantiomerically enriched sec-alcohols in some extent of optical yields (up to 51% ee). (C) 1999 Elsevier Science Ltd . All rights reserved.