Synthesis and conformational analysis of carbasugar bioisosteres of α-l-iduronic acid and its methyl glycoside
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference52 articles.
1. Evidence for conformational equilibrium of the sulfated L-iduronate residue in heparin and in synthetic heparin mono- and oligo-saccharides: NMR and force-field studies
2. Conformational equilibria of α-L-iduronate residues in disaccharides derived from heparin
3. Conformer populations of l-iduronic acid residues in glycosaminoglycan sequences
4. The anticoagulant activation of antithrombin by heparin
5. Synthesis of Conformationally Lockedl-Iduronic Acid Derivatives: Direct Evidence for a Critical Role of the Skew-Boat2S0 Conformer in the Activation of Antithrombin by Heparin
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2. Oxocarbenium ion cyclizations for the synthesis of disaccharide mimetics of 2-amino-2-deoxy-pyranosides: Application to the carbasugar of β-galactosamine-(1,4)-3-O-methyl-D-chiro-inositol;Carbohydrate Research;2022-08
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