Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000083.xml
Synlett 1996; 1996(2): 169-170
DOI: 10.1055/s-1996-5362
DOI: 10.1055/s-1996-5362
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.
Efficient Syntheses of Amadori Rearrangement Compounds
Further Information
Publication History
Publication Date:
31 December 2000 (online)
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.
amadori rearrangement compound - 1-amino-1-deoxy-2-ketose - reductive amination - deprotection