Preparation of acetylated 2-heptulo- and 2-hexulo-pyranosononitriles from acetylated 1-bromo-d-glycosyl cyanides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference8 articles.
1. Bromination of acetylated 2,5-anhydro-aldononitriles at the anomeric centre using N-bromosuccinimide: synthesis of 2,3,4,6-tetra-O-acetyl-1-bromo-d-galactopyranosyl cyanide and its d-xylopyranosyl analogue
2. Preparation of acetylated C-(1-bromo-d-glycosyl) heterocycles and 1-bromo-d-glycosyl cyanides
3. Functionalization at Proanomeric Centres by Photobromination. A Novel Access to Oxo- and Acyloxyimino-glycosyl Bromides
4. C-5 bromination of some glucopyranuronic acid derivatives
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1. Structure of C-1 substituted glycopyranosyl azides: new insights based on CD measurements;Tetrahedron: Asymmetry;1999-03
2. Synthesis and some transformations of 1-azido-glycopyranosyl cyanides-precursors of anomeric α-amino acids;Tetrahedron;1996-07
3. Preparation and photolysis of 1-cyano-glycopyranosyl azides;Tetrahedron Letters;1995-05
4. Stereoselective bromination of β-ribofuranosyl amide. Enantioselective synthesis of (+)-hydantocidin;Tetrahedron Letters;1994-07
5. Synthesis of C-glycosyltetrazoles related to 3-deoxy-D-arabino-heptulosonic acid 7-phosphate (DAHP); potential inhibitors of early steps in the shikimate pathway;Journal of the Chemical Society, Perkin Transactions 1;1992
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