2-STEP STEREOSELECTIVE CONVERSION OF 5-MONOSUBSTITUTED 1,3-DIOXOLAN-4-ONES INTO SELECTIVELY PROTECTED 2,3-ERYTHRO-1,2,3-TRIOLS - A ROUTE TOPOLYHYDROXYLATED MOLECULES

Authors
UNTERSTELLER E XIN YC SINAY P
Citation
E. Untersteller et al., 2-STEP STEREOSELECTIVE CONVERSION OF 5-MONOSUBSTITUTED 1,3-DIOXOLAN-4-ONES INTO SELECTIVELY PROTECTED 2,3-ERYTHRO-1,2,3-TRIOLS - A ROUTE TOPOLYHYDROXYLATED MOLECULES, Tetrahedron letters, 35(16), 1994, pp. 2537-2540
Citations number
34
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
35
Issue
16
Year of publication
1994
Pages
2537 - 2540
Database
ISI
SICI code
0040-4039(1994)35:16<2537:2SCO51>2.0.ZU;2-1
Abstract
5-Monosubstituted 1,3-dioxolan-4-one 1 are stereoselectively converted into selectively protected 2,3-erythro-1,2,9-triols 3 via Tebbe methy lenation, followed by hydroboration-oxidation.