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Eisai Co., Ltd., Tsukuba Research Laboratories | 論文
- A Practical Synthesis of Optically Active Platelet-Activating Factor Antagonist, (+)-6-(2-Chlorophenyl)-3-cyclopropanecarbonyl-8,11-dimethyl-2,3,4,5-tetrahydro-8H-pyrido[4', 3' : 4,5]thieno[3,2-f][1,2,4]triazolo[4,3-a][1,4]diazepine (E6123), and Its Absol
- Structure-Activity Studies on Triazolothienodiazepine Derivaties as Platelet-Activating Factor Antagonists
- Synthesis of a New Dual Metalloprotease Inhibitor. II. Stereoselective Synthesis of Peptidomimetic [5.7]-Bicyclic Compounds
- Synthesis of a New Dual Metalloprotease Inhibitor. I. Diastereoselective Alkylation of Protected 6-Oxopipecolic Acid Esters
- Hapten Synthesis for (+)-6-(2-Chlorophenyl)-3-cyclopropanecarbonyl-8,11-dimethyl-2,3,4,5-tetrahydro-8H-pyrido[4', 3' : 4,5]thieno[3,2-f]triazolo[4,3-a][1,4]diazepine(E6123)
- A Practical Synthetic Method for 3-(N, N-Disubstituted Carbamoyloxy)-methyl Cephems without Generating the Δ^2-Isomers
- Studies on the Stability of Δ^2 and Δ^3 Cephem Esters. I. Marked Difference in Stability between Δ^2 and Δ^3 Cephem Prodrug Esters and Application to the Preparation of Key Intermediates for Oral Cephem Synthesis
- Studies on the Stability of Δ^2 and Δ^3 Cephem Esters. II.Comparative Stability Studies of Δ^2 and Δ^3 Cephems at Various pHs and the Degradation Process of Δ^2 Caphem Esters
- Synthesis of α-Tocopherol: Scandium(III) Trifluoromethanesulfonate as an Efficient Catalyst in the Reaction of Hydroquinone with Allylic Alcohol
- Tin(II) Chloride Catalyzed Synthesis of β-D-Ribonucleosides
- Catalytic Stereoselective Synthesis of β-Ribonucleosides from Mthyl Ribofuranosyl Carbonate and Trimethylsilylated Nucleoside Bases by Combined Use of Silver Salts and Diphenyltin Sulfide
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