Synthesis of the optically active 4-O-phosphono-d-glucosamine derivatives related to the nonreducing-sugar subunit of bacterial lipid A

This publication has 20 references indexed in Scilit:

• Synthesis of 1,5-Anhydro- 2-deoxy- 4-O-phosphono-3-O-tetradecanoyl-2-[(3R)- and (3S)-3-Tetradecanoyloxytetradecanamido]-D-glucitol (GLA-40) Related to Bacterial Lipid A
  Journal of Carbohydrate Chemistry, 1986
• Synthesis of 2-deoxy-4-O-phosphono-3-O-tetradecanoyl-2-[(3R- and (3S)-3-tetradecanoyloxytetradecanamido]-d-glucose: a diastereoisomeric pair of 4-O-phosphono-d-glucosamine derivatives (GLA-27) related to bacterial lipid A
  Carbohydrate Research, 1986
• Structural requirements for inducing in vitro B lymphocyte activation by chemically synthesized derivatives related to the nonreducing D‐glucosamine subunit of lipid A
  European Journal of Immunology, 1986
• Comparison of Murine B Cell Clonal Expansions by Synthetic Lipid A and Muramyl Dipeptide Analogs
  Microbiology and Immunology, 1985
• Synthetic and natural Escherichia coli free lipid A express identical endotoxic activities
  European Journal of Biochemistry, 1985
• B cell activation and adjuvant activities of chemically synthesized analogues of the nonreducing sugar moiety of lipid A
  European Journal of Immunology, 1985
• Biological activities of chemically synthesized analogues of the nonreducing sugar moiety of lipid A
  FEBS Letters, 1984
• Synthesis of biologically active, novel monosaccharide analogs of lipid A.
  Agricultural and Biological Chemistry, 1984
• Molecular requirements for B-lymphocyte activation by Escherichia coli lipopolysaccharide.
  Proceedings of the National Academy of Sciences, 1983
• Chemical structure and biological activities of lipid A's from various bacterial families
  The Science of Nature, 1978