ASYMMETRIC REDUCTION OF KETO OXIME ETHERS USING OXAZABOROLIDINE REAGENTS - THE ENANTIOSELECTIVE SYNTHESIS OF CYCLIC AMINO-ALCOHOLS

Authors
TILLYER RD BOUDREAU C TSCHAEN D DOLLING UH REIDER PJ
Citation
Rd. Tillyer et al., ASYMMETRIC REDUCTION OF KETO OXIME ETHERS USING OXAZABOROLIDINE REAGENTS - THE ENANTIOSELECTIVE SYNTHESIS OF CYCLIC AMINO-ALCOHOLS, Tetrahedron letters, 36(25), 1995, pp. 4337-4340
Citations number
23
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
36
Issue
25
Year of publication
1995
Pages
4337 - 4340
Database
ISI
SICI code
0040-4039(1995)36:25<4337:AROKOE>2.0.ZU;2-6
Abstract
Asymmetric reduction of keto oxime ethers 2 catalyzed by oxazaborolidi ne-borane complex 4 produces the cia amino alcohols 1 efficiently and with high levels of diastereo- and enantioselectivity.