DIASTEREOSELECTIVE HYDRIDE REDUCTIONS OF ALPHA-HYDROXY OXIMINO ETHERS- SYNTHESIS OF SYN-1,2-AMINO ALCOHOLS

Authors
WILLIAMS DR OSTERHOUT MH REDDY JP
Citation
Dr. Williams et al., DIASTEREOSELECTIVE HYDRIDE REDUCTIONS OF ALPHA-HYDROXY OXIMINO ETHERS- SYNTHESIS OF SYN-1,2-AMINO ALCOHOLS, Tetrahedron letters, 34(20), 1993, pp. 3271-3274
Citations number
10
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
34
Issue
20
Year of publication
1993
Pages
3271 - 3274
Database
ISI
SICI code
0040-4039(1993)34:20<3271:DHROAO>2.0.ZU;2-N
Abstract
Tetramethylammonium triacetoxyborohydride provides for the stereocontr olled reduction of alpha-hydroxy-E/Z-oximino ethers to yield syn-1,2-a mino alcohols.