Synthesis of an analogue of the antithrombin binding region of heparin containing α‐L‐idopyranose
- 1 January 1987
- journal article
- Published by Wiley in Recueil des Travaux Chimiques des Pays-Bas
- Vol. 106 (11) , 593-595
- https://doi.org/10.1002/recl.19871061108
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Conformational analysis of synthetic heparin‐like oligosaccharides containing α‐L‐idopyranosyluronic acidRecueil des Travaux Chimiques des Pays-Bas, 1987
- Synthesis of an antithrombin binding heparin-like pentasaccharide lacking 6-0 sulphate at its reducing end.Tetrahedron Letters, 1986
- Evidence for conformational equilibrium of the sulfated L-iduronate residue in heparin and in synthetic heparin mono- and oligo-saccharides: NMR and force-field studiesJournal of the American Chemical Society, 1986
- D-Idose: a one- and two-dimensional NMR investigation of solution composition and conformationThe Journal of Organic Chemistry, 1986
- Synthesis of a Pentasaccharide Corresponding to the Antithrombin III Binding Fragment of HeparinJournal of Carbohydrate Chemistry, 1985
- Structure and Biological Activity of HeparinAdvances in Carbohydrate Chemistry and Biochemistry, 1985
- Total synthesis of a heparin pentasaccharide fragment having high affinity for antithrombin IIICarbohydrate Research, 1984
- Hexopyranose sugars conformation revisedTetrahedron, 1984