中山清 | Exploratory Research Laboratories I, Daiichi Pharmaceutical Co. Ltd.,

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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
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

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