スポンサーリンク
Department of Applied Chemisty, Osaka Prefecture University | 論文
- Synthesis of [2]- and [3]Rotaxanes by an End-Capping Approach Utilizing Urethane Formation
- Syntheses of [60]Fullerene and N, N-Bis(4-biphenyl)aniline-Tethered Rotaxane : Photoinduced Electron-Transfer Processes via Singlet and Triplet States of [60]Fullerene
- Photoreaction of Cinnamate with Nitrogen Monoxide Catalyzed by Metallosalen Complexes
- Polyslipping: A New Approach to Polyrotaxane-like Assemblies
- Chemical Modification of Amide-Based Catenanes and Rotaxanes I. Synthesis of secondary Amine [2]Catenanes and [2]Rotaxanes by theBorane Reduction of secondary Amide[2]Catenanes and [2]Rotaxanes and Mobility of Their Components
- "Unlock-Lock" Approach to [2] and [3]Rotaxanes:Entering of a Ring through Disulfide Linkage That is Unlocked by Thiol "Key"
- Synthesis and Structure of [2]Catenated tertiary Octamide and Octamine
- Conjugate Addition - Approach to End - Capping of Pseudorotaxanes for Rotaxane Synthesis
- Radically Polymerizable Pseudorotaxane Monomers : Versatile Building Units for Side Chain Polyrotaxane Synthesis
- A Catenated Cyclic Octamine : A Noncovalently Bonded Molecular System without Attractive Interaction between the Two Units
- A Rational Design of Helix: Absolute Helix Synthesis by Binaphthyl-Salen Fusion
- Facile Routes to Ru(η^3-Allyl)(NO)(PPh_3)_2 Complexes via Hydrometallation of RuH(NO)(PPh_3)_3 to 1, 3-Butadienes and Allenes
- Dynamic Covalent Chemistry in Rotaxane Synthesis. Slipping Approach to [2] Rotaxane Utilizing Reversible Cleavage-Rebondage of Trityl Thioether Linkage
- Rotaxane Synthesized by End-capping via Hydroruthenation of Axle Terminal Acetylene and Its Derivation to η^3-Allylruthenium Complex-containing Rotaxane
- Synthesis of (+)-Turmeronol A, an Inhibitor of Soybean Lipoxygenase, and (+)-ar-Turmerone
- Synthesis of Diarylsulfoximines by the Friedel-Crafts Reaction of Sulfonimidoyl Chlorides
- Synthesis and Structure of Optically Active Helical Poly- and Oligocarbonates Consisting of C_2-Chiral Biphenyl Unit
- Optically Active Poly-and Oligo(biphenyl carbonate)s as Stable Helical Molecules
- An α-Carboline-containing Host Material for High-efficiency Blue and Green Phosphorescent OLEDs