REARRANGEMENTS OF O-PROTECTED GLYCOSYLENAMINES - A NEW AND EFFICIENT ROUTE FOR THE SYNTHESIS OF O-PROTECTED 4-AMINOALDOSES

Citation
Ma. Pradera et al., REARRANGEMENTS OF O-PROTECTED GLYCOSYLENAMINES - A NEW AND EFFICIENT ROUTE FOR THE SYNTHESIS OF O-PROTECTED 4-AMINOALDOSES, Tetrahedron letters, 36(47), 1995, pp. 8653-8656
Citations number
13
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00404039
Volume
36
Issue
47
Year of publication
1995
Pages
8653 - 8656
Database
ISI
SICI code
0040-4039(1995)36:47<8653:ROOG-A>2.0.ZU;2-M
Abstract
O-Protected 4-deoxy-4-diethoxycarbonylvinylaminoaldoses with D-galacto , L-arabino and L-lyxo configurations (3) are prepared by a nucleophil ic rearrangement of easily available glycosylamine derivatives