Hattori Kenjiro | Department Of Applied Chemistry Faculty Of Engineering Tokyo Institute Of Polytechnics
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概要
関連著者
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Hattori Kenjiro
Department Of Applied Chemistry Faculty Of Engineering Tokyo Institute Of Polytechnics
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TODA Fujio
Department of Bioengineerig, Faculty of Bioscience and Biotechnology, Tokyo Institute of Technology
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Takahashi Keiko
Department Of Applied Chemistry Faculty Of Engineering Tokyo Institute Of Polytechnics
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TAKAHASHI Keiko
Department of Biochemistry, Showa University School of Medicine
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YAMANOI Takashi
The Noguchi Institute
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Hattori Kenjiro
Department Of Nanochemistry Faculty Of Engineering Tokyo Polytechnic University
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ODA Yoshiki
The Noguchi Institute
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MIURA Masumi
The Noguchi Institute
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Miura Masumi
The Noguchi Institute:department Of Nanochemistry Faculty Of Engineering Tokyo Polytechnic Universit
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Yamamoto Yasuhiko
Department Of Biochemistry And Molecular Vascular Biology Kanazawa University Graduate School Of Med
著作論文
- Hydrolytic Catalysis with Complexation by Modified Cyclodextrins Having Diastereomeric Structure
- The Effects of Cyclodextrins on the Reduction of Ninhydrin with N-Alky1-1, 4-dihydronicotinamides
- Chiral Recognition in the Inclusion Complex of Cyclodextrins with N-Dansyl-Phenylalanine Observed by Linked Scan FAB-MS Spectrometry
- Syntheses and Doxorubicin-Inclusion Abilities of β-Cyclodextrin Derivatives with a Hydroquinone α-Glycoside Residue Attached at the Primary Side
- Synthesis and Isolation of Regiospecific Mono Iodo-Cyclodextrin as a Fragile Intermediate to Amino-Cyclodextrin
- Syntheses and Doxorubicin-Inclusion Abilities of β-Cyclodextrin Derivatives with a Hydroquinone α-Glycoside Residue Attached at the Primary Side
- Spacer-assisted catalytic action of imidazole-appended .GAMMA.-cyclodextrin.
- The Synthesis of the Polymer Containing the Si-O-phenylene Bond, using Transition Metal Salts as Catalysts
- The regiospecific mono tosylation of cyclodextrins.
- 1H NMR study of conformation of formyl-L-phenylalanyl-6-deoxy-6-amino-cyclomaltoheptaose that has excellent ability of chiral recognition.