Efficient Syntheses of Amadori Rearrangement Compounds
- 1 February 1996
- journal article
- letter
- Published by Georg Thieme Verlag KG in Synlett
- Vol. 1996 (02) , 169-170
- https://doi.org/10.1055/s-1996-5362
Abstract
Various types of 1-amino-1-deoxy-2-ketoses, Amadori rearrangement compounds, have bee synthesized using a reduction amination of the 1-formyl derivative (3), prepared from 2,3:4,5-di-O-isopropylidene-D-fructopyranose (2), with unprotected or partially protected amino acids in a few steps.Keywords
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