EFFICIENT SYNTHESES OF AMADORI REARRANGEMENT COMPOUNDS

Authors
IWAMOTO T KAN T KATSUMURA S OHFUNE Y
Citation
T. Iwamoto et al., EFFICIENT SYNTHESES OF AMADORI REARRANGEMENT COMPOUNDS, Synlett, (2), 1996, pp. 169-170
Citations number
13
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synlett → ACNP
ISSN journal
09365214
Issue
2
Year of publication
1996
Pages
169 - 170
Database
ISI
SICI code
0936-5214(1996):2<169:ESOARC>2.0.ZU;2-Q
Abstract
Various types of 1-amino-1-deoxy-2-ketoses, Amadori rearrangement comp ounds, have been synthesized using a reductive amination of the 1-form yl derivative (3), prepared from 2,3:4,5-di-O-isopropylidene-D-fructop yranose (2), with unprotected or partially protected amino acids in a few steps.