A HIGHLY DIASTEREOSELECTIVE SYNTHESIS OF ALPHA-SUBSTITUTED-BETA-HYDROXY COMPOUNDS FROM CORRESPONDING BETA-STANNYL COMPOUNDS

Authors
YAMAMOTO M ITOH K KISHIKAWA K KOHMOTO S
Citation
M. Yamamoto et al., A HIGHLY DIASTEREOSELECTIVE SYNTHESIS OF ALPHA-SUBSTITUTED-BETA-HYDROXY COMPOUNDS FROM CORRESPONDING BETA-STANNYL COMPOUNDS, Chemistry Letters, (10), 1997, pp. 1035-1036
Citations number
16
Categorie Soggetti
Chemistry
Journal title
Chemistry Letters → ACNP
ISSN journal
03667022
Issue
10
Year of publication
1997
Pages
1035 - 1036
Database
ISI
SICI code
0366-7022(1997):10<1035:AHDSOA>2.0.ZU;2-9
Abstract
Anti-beta-stannyl-alpha-substituted carbonyl compounds were completely converted to its syn-analogues, and each diastereomer was oxidized to its beta-hydroxylated analogues with retention of the stereochemistry .