Yamashita K | Department Of Chemical Science And Technology Faculty Of Engineering The University Of Tokushima

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著作論文

Conformational Analysis of the NMDA Receptor Antagonist (1S,2R)-1-Phenyl-2-[(S)-1-aminopropyl]-N,N-diethylcyclopropanecarboxamide (PPDC) Designed by a Novel Conformational Restriction Method Based on the Structural Feature of Cyclopronane Ring
New Neplanocin Anallogues. VIII. Synthesis and Biological Activity of 6'-C-Ethyl, -Ethenyl, and -Ethynyl Derivatives of Neplanocin A
Regioselective Synthesis of 6-Alkyl- and 6-Prenylpolyhydroxyisoflavones and 6-Alkylcoumaronochromone Derivatives
Studies of the Selective O-Alkylation and Dealkylation of Flavonoids. XXIV. A Convenient Method for Synthesizing 6- and 8-Methoxylated 5,7-Dihydroxyisoflavones
Studies of the Selective O-Alkylation and Dealkylation of Flavonoids. XXIII. Demethylation Behaviors of 6-Hydroxy-4', 7-dimethoxy-5-tosyloxyflavones with Anhydrous Aluminum Halides in Acetonitrile
Studies of the Selective O-Alkylation and Dealkylation of Flavonoids. XXII. A Convenient Method for Synthesizing 3,5,7-Trihydroxy-6-methoxyflavones
Studies of the Selective O-Alkylation and Dealkylation of Flavonoids. XXI.^ A Convenient Method for Synthesizing 3,5,7-Trihydroxy-6,8-dimethoxyflavones and 5,7-Dihydroxy-3,6,8-trimethoxyflavones
Studies of the Selective O-Alkylation and Dealkylation of Flavonoids. XX. A Convenient Method for Synthesizing 5,6,7-Trihydroxyisoflavones and 5,6-Dihydroxy-7-methoxyisoflavones
Studies of the Selective O-Alkylation and Dealkylation of Flavonoids. XVIII.^ A Convenient Method for Synthesizing 3,5,6,7-Tetrahydroxyflavones

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