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Exploratory Research Laboratories I, Daiichi Pharmaceutical Co. Ltd., | 論文
- Zinc Triflate-Promoted Glycosidation : Synthesis of Lipid A Disaccharide Intermediates
- A Useful Method for Deprotection of the Protective Allyl Group at the Anomeric Oxygen of Carbohydrate Moieties Using Tetrakis(triphenylphosphine)palladium
- Direct Transformation of O-Glycosides into Other O-Glycosides Using Trimethylsilyl Bromide and Zinc Bromide
- Synthesis and Biological Activities of Lipid A Analogs : Modification of a Glycosidically Bound Group with Chemically Stable Polar Acidic Groups and Lipophilic Groups on the Disaccharide Backbone with Tetradecanoyl or N-Dodecanoylglycyl Groups
- Direct Transformation of O-Glycoside into Glyosyl Bromide with the Combination of Trimethylsilyl Bromide and Zinc Bromide
- Synthesis and Biological Activities of Analogs of a Lipid A Biosynthetic Precursor : 1-O-Phosphono-oxyethyl-4'-O-phosphono-disaccharides with (R)-3-Hydroxytetradecanoyl or Tetradecanoyl Groups at Positions 2,3,2' and 3'
- A Novel Glycoside Anomerization Catalyzed by Trimethylsilyl Bromide and Zinc Bromide in Combination
- Synthesis and Antitumor Activity of Lipid A Analogs Having a Phosphonooxyehyl Group with α- or β-Configuration at Position 1
- Novel Stereoselective Glycosidation by the Combined Use of Trityl Halide and Lewis Acid
- Synthesis and Antiallergy Activity of [1,3,4]Thiadiazolo[3,2-α]-1,2,3-triazolo[4,5-d]pyrimidin-9(3H)-one Derivatives. II. 6-Alkyl- and 6-Cycloalkylalkyl Derivatives
- Facile Total Synthesis of Carbonolides by Witting-Hoener Macro-Cyclization and Stereoselective Epoxidation