Syntheses and Doxorubicin-Inclusion Abilities of β-Cyclodextrin Derivatives with a Hydroquinone α-Glycoside Residue Attached at the Primary Side
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概要
- 論文の詳細を見る
- 2009-01-01
著者
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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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Hattori Kenjiro
Department Of Applied Chemistry Faculty Of Engineering Tokyo Institute Of Polytechnics
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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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- Synthesis and Isolation of Regiospecific Mono Iodo-Cyclodextrin as a Fragile Intermediate to Amino-Cyclodextrin
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- Syntheses and Doxorubicin-Inclusion Abilities of β-Cyclodextrin Derivatives with a Hydroquinone α-Glycoside Residue Attached at the Primary Side
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- 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.