スポンサーリンク
Faculty of Pharmaceutical Sciences, Osaka University | 論文
- Synthesis and Antiviral Activities of Carbocyclic Oxetanocin Analogues
- Syntheses of Arylacetone and Arylacetonitrile by Friedel-Crafts Reaction with α-Chloro-α-(methylthio)-substituted Acetone and Acetonitrile
- Phytochemical Studies on Meliaceous Plants. VII. The Structures of Two New Ionone Glucosides from Melia toosendan SIEB. et ZUCC. and a Novel Type of Selective Biooxidation by a Kind of Protease
- Total Synthesis of Securinine
- Studies on Transfer Ribonucleic Acids and Related Compounds. XXXIV. Stepwise Diester or Partial Triester Synthesis of Penta-to Octanucleotides Corresponding to Residues 41-46,47-54,61-65 and 66-71 of tRNA^_f of E. coli
- Studies on Transfer Ribonucleic Acids and Related Compounds. XXV. Synthesis of E. coli tRNA^_f 5'-Terminal Tetranucleotide C-G-C-Gp and Its Sequence Analog U-G-C-Gp
- Studies on Transfer Ribonucleic Acids and Related Compounds. XVII. Studies on Protecting Groups of Trisubstituted Phosphates in the Synthesis of Ribooligonucleotides
- Synthetic Studies on Aphidicolane and Stemodane Diterpenes. V. A Facile Formal Total Synthesis of (±)-Aphidicolin via a Lewis Acid-Mediated Stereoselective Spiroannelation
- Lewis Acid-Mediated Stereoselective Spiroannelation : A Facile Access to Aphidicolane and Stemodane B/C/D Ring Systems
- Synthetic Studies on Aromadendrane-Type Compounds. II.Stereoselective Synthesis of (+)-1,2-Didehydroaromadendrane
- Synthetic Studies on Aromadendrane-Type Compounds. I. Stereoselective Construction of Aromadendrane- and Alloaromadendrane-Type Skeletons
- Construction of Asymmetric Quaternary Carbon Center Containing Heteroatom via Regioselective Cleavage of Cyclopropane Ring Mediated by Mercury(II) Salt
- Synthetic Study on Gymnomitrol. II. A Synthesis of (±)-Isogymnomitrol
- 57 アロマデンドラン型化合物の不斉合成研究(ポスター発表の部)
- Synthetic Study on Gymnomitrol and Related Compounds. I.Preparation and Cyclopropane Ring Opening of 1,2,6-Trimethyltetracyclo[5.3.1.0^.0]undecan-9-one
- 7,7-Dimethyltricyclo[3.3.0.0^]octan-3-ones as Synthetic Intermediates. VI. An Improved Formal Synthesis of (±)-Descarboxyquadrone via Highly Regioselective Cyclopropane Ring Opening of Tricyclo[3.3.0.0^]octan-3-one
- An Efficient p-Thiocyanation of Phenols and Naphtols Using a Reagent combination of Phenyliodine Dichloride and Lead(II) Thiocyanate
- ORGANIC SYNTHESIS UTILIZING BECKMANN FRAGMENTATION : ASYMMETRIC CARBON-CARBON BOND FORMATION VIA CHIRAL ACETAL INTERMEDIATES
- Organic Synthesis Utilizing the Intermediates in Beckmann Fragmentation of α-Alkoxyketoximes
- Asymmetric Synthesis of Anthracyclinones : Synthesis of a New Chiral AB-Synthon, (5R, 6R)-6-Ethyl-5,6-dihydroxy-5,6,7,8-tetrahydro-1,4-naphthoquinone, and Its Application for a Novel Regioselective Synthesis of (-)-γ-Rhodomycinone
スポンサーリンク