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Central Research Division, Takeda Chemical Industries, Ltd. | 論文
- Structure of Tauranin and a Note on the "C_-Acids" obtained from Di- and Triterpenoids
- Synthesis of Salmon Endorphin
- The Use of N-Hydroxy-5-norbornene-2,3-dicarboximide Active Esters in Peptide Synthesis
- A New Route to Semisynthetic Cephalosporins from Deacetylcephalosporin C. I. Synthesis of 3-Heterocyclicthiomethyl-cephalosporins
- Synthesis of Dibenzo [b, f] cycloprop [d] azepine Derivatives. II. Introduction of a Cyclopropane Ring by the Dichloromethylene Transfer Reaction
- Synthesis of Dibenzo [b, f] cycloprop [d] azepine Derivatives. I. Introduction of a Cyclopropane Ring by the Use of Simmons-Smith Reagent
- Spirocyclopropane Compounds. V. One-Step Synthesis of 5-Acetylspiro [benzofuran-2 (3H), 1'-cyclopropan]-3-one
- Spirocyclopropane Compounds. II. Synthesis and Biological Activities of Spiro [cyclopropane-1,2'-[2H] indol]-3'(1'H)-ones
- Photochemical Reaction of 21-Methyl-20,21-diketosteroids : The Formation of New 3´, 4´, 16α, 17α-Tetrahydrocyclobut [16,17] androstanes
- Synthesis and Anti-inflammatory Activity of Steroidal 17-Yl-α-Oxothiocarboxamides and Related Compounds
- Steroid [16,17-c]isoxazoline
- Synthesis of 20α-Hydroxy-16-oxosteroids and the C-20 Configuration of Δ^-16-Ocosteroids
- Aldol Condensation of Corticoids with Formaldehyde. II. 21-Hydroxymethylation of Reichstein's Substance S, Dexamethasone and Deoxycorticosterone
- 4.制癌性抗生物貭Chromomycin A_3の化学構造
- Aldol-Condensation of Corticoids with Formaldehyde. Syntheses of 21-Hydroxy-methyl-corticoids and 21-Methyl-11β, 17α-dihydroxy-pregna-1,4-diene-3,20,21-trione 17-Acetate.
- Studies on Azetidine Derivatives. IV. Synthesis and Some Reactions of Azetidin-3-one Derivatives
- Studies on Heterocyclic Compounds. VI. Syntheses of Oudenone and Its Related Compounds. (1)
- Heterocycles. VI. Syntheses of 4H-s-Triazolo [4,3-a] [1,4] benzodiazepines, Novel Tricyclic Psychosedatives
- Synthesis of Some Di-and Tri-Substituted Analogs of Luteinizing Hormone Releasing Hormone (LH-RH)
- Isobornyloxycarbonyl Function, a New Convenient Amino-Protecting Group in Peptide Synthesis.IV. Synthesis of Gonadotropin-Releasing Hormone (Gn-RH or LH-RH/FSH-RH)
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