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4. Synthesis of heparin fragments. A chemical synthesis of the pentasaccharide O-(2-deoxy-2-sulfamido-6-O-sulfo-alpha-D-glucopyranosyl)-(1-4 )-O-(beta-D-glucopyranosyluronic acid)-(1-4)-O-(2-deoxy-2-sulfamido-3,6-di-O-sulfo-alpha-D-glu copyranosyl)-(1-4)-O-(2-O-sulfo-alpha-L-idopyranosyluronic acid)-(1-4)-2-deoxy-2-sulfamido-6-O-sulfo-D-glucopyranose decasodium salt, a heparin fragment having high affinity for antithrombin III. Petitou M, Duchaussoy P, Lederman I, Choay J, Sinaÿ P, Jacquinet JC, Torri G. Carbohydr Res; 1986 Mar 15; 147(2):221-36. PubMed ID: 3708627 [Abstract] [Full Text] [Related]
5. Binding of heparin to antithrombin III: a chemical proof of the critical role played by a 3-sulfated 2-amino-2-deoxy-D-glucose residue. Petitou M, Duchaussoy P, Lederman I, Choay J, Sinaÿ P. Carbohydr Res; 1988 Aug 15; 179():163-72. PubMed ID: 3208245 [Abstract] [Full Text] [Related]
6. [Synthesis of trisaccharide determinants of enterobacterial common antigens]. Paulsen H, Lorentzen JP. Carbohydr Res; 1986 Aug 01; 150():63-90. PubMed ID: 2428497 [Abstract] [Full Text] [Related]
7. [Synthesis of the pentasaccharide chain of the Forsman antigen]. Paulsen H, Bünsch A. Carbohydr Res; 1982 Mar 01; 100():143-67. PubMed ID: 7083250 [Abstract] [Full Text] [Related]
8. Glycosidation of 2,5-anhydro-3,4-di-O-benzyl-D-mannitol with different glucopyranosyl donors: a comparative study. Tegdes A, Medgyes G, Boros S, Kuszmann J. Carbohydr Res; 2006 May 01; 341(6):776-81. PubMed ID: 16473342 [Abstract] [Full Text] [Related]
11. 2,3,4-Tri-O-acetyl-1,6-anhydro-beta-D-mannopyranose, an artifact produced during carbohydrate analysis. A total synthesis of 2,3,5-tri-O-acetyl-1,6-anhydro-beta-D-mannofuranose. Manna S, McAnalley BH, Ammon HL. Carbohydr Res; 1993 Apr 23; 243(1):11-27. PubMed ID: 8324757 [Abstract] [Full Text] [Related]
17. Synthesis of a cyanoethylidene derivative of 3,6-anhydro-d-galactose and its application as glycosyl donor. Vogel C, Torres GM, Reinke H, Michalik D, Voss A. Carbohydr Res; 2007 Feb 26; 342(3-4):520-8. PubMed ID: 17056018 [Abstract] [Full Text] [Related]