Synthesis of a peripheral trisaccharide sequence of lutropin, a pituitary glycoprotein hormone; use of chitobiose as a key starting material

This publication has 16 references indexed in Scilit:

• Peracetylated chitobiose: Preparation by specific degradations of chitin, and chemical manipulations
  Carbohydrate Research, 1989
• 1,6-Anhydro-β-maltotriose: Preparation from pullulan, and regioselective partial-protection reactions
  Carbohydrate Research, 1989
• Synthesis of a new antimicrobial aminoglycoside employing maltose as a key starting material
  Tetrahedron Letters, 1987
• Synthesis of methyl glycoside derivatives of tri- and penta-saccharides related to the antithrombin III-binding sequence of heparin, employing cellobiose as a key starting-material
  Carbohydrate Research, 1987
• Synthesis of oligosaccharide structures unique to pituitary glycoprotein hormones
  Canadian Journal of Chemistry, 1987
• Synthesis of a heparin pentasaccharide fragment with a high affinity for antithrombin III employing cellobiose as a key starting material
  Tetrahedron Letters, 1986
• Synthesis of “dihydroacarbose”, a potent α-d-glucosidase inhibitor
  Carbohydrate Research, 1986
• Discrimination between the 2,3- and the 2′,3′-hydroxyl groups of maltose and cellobiose through their specific protection
  Carbohydrate Research, 1985
• Synthesis of amylostatin (XG), α-glucosidase inhibitor with basic pseudotrisaccharide structure
  Tetrahedron Letters, 1982
• A modified procedure for the synthesis of 1,6-anhydro disaccharides
  Carbohydrate Research, 1982