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Medicinal Chemistry Research Laboratories Sankyo Co. Ltd. | 論文
- Syntheses of 3,4-Epoxy- and 3,4-Epimino-pyrrolidines
- Synthesis of 4,5-Epiminotetrahydro-1,2-oxazine
- Syntheses of 3,4-Epiminopyrrolidine and 4,5-Epiminotetrahydro-1,2-oxazine
- Syntheses of Some Branched-chain Nitrocycloalkanols
- 1,3-Dipolar Cycloaddition Reaction of Aziridinedicarboximide
- Syntheses of Tricyclic Amines from Azabicyclic Compounds through Carbenes
- Studies on Orally Active Cephalosporin Esters. V. : A Prodrug Approach for Oral Delivery of 3-Thiazoliomethyl Cephalosporin
- Studies on Penem and Carbapenem. II. : An Improved Synthesis of Orally Active Penem Antibiotic (5-Methyl-2-oxo-1,3-dioxol-4-yl)methyl (5R, 6S)-2-(2-Fluoroethylthio)-6-[(1R)-1-hydroxyethyl]penem-3-carboxylate
- Synthesis and Structure-activity Relationships of Novel Parenteral Carbapenems, CS-023 (R-115685) and Related Compounds Containing an Amidine Moiety
- Synthesis and Antibacterial Activity of Novel 1β-Methyl Carbapenems with Cycloalkylamine Moiety at the C-2 Position
- Synthesis and Biological Evaluation of Novel Tricyclic Carbapenems (Trinems)
- Efficient Syntheses of(S)-4-Hydroxy-2-pyrrolidinone Derivatives
- Synthesis and Biological Evaluation of New Oral Carbapenems with 1-Methyl-5-oxopyrrolidin-3-ylthio Moiety
- Synthesis and Structure-activity Relationships of 1β-Methylcarbapenems with Quaternary Ammonium Side Chains
- A Novel Oral Carbapenem CS-834:Chemical Stability of Pivaloyloxymethyl Esters of Carbapenems and Cephalosporins in Phosphate Buffer Solution
- Synthesis and Structure-activity Relationships of a Novel Oral Carbapenem. CS-834
- Two-dimensional Gel Electrophoresis of Ribosomal Proteins as a Novel Approach to Bacterial Taxonomy : Application to the Genus Arthrobacter
- A Novel Heterocyclic Compound. Synthesis and Reactivities of an Oxazolo[3,2-a]thieno[3,2-d]pyrimidine Derivative
- Studies on Orally Active Cephalosporin Esters. IV. : Effect of the C-3 Substituent of Cephalosporin on the Gastrointestinal Absorption in Mice
- Studies on High-energy Collision-induced Dissociation of Endogenous Cannabinoids : 2-Arachidonoylglycerol and N-Arachidonoylethanolamide in FAB-Mass Spectrometry
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