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Toshio Furuya

Tohoku University

36

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206

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Novel 5-Hydroxytryptamine (5-HT3) Receptor Antagonists. Part 3. Pharmacological Evaluations and Molecular Modeling Studies of Optically Active 4,5,6,7-Tetrahydro-1H-benzimidazole Derivatives.

2010 ChemInform
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[In-silico approaches for fragment-based drug design].

2010 Yakugaku Zasshi-journal of The Pharmaceutical Society of Japan
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Chemical Shift Assignment of Ca2+/calmodulin (1H, 13C, and 15N) Complexed with Its Binding Domain from Rat Ca2+/calmodulin Dependent Protein Kinase Kinase (1H).

2007 Journal of Back and Musculoskeletal Rehabilitation
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α−メチル−１，３−ベンゼンジオキソール−５−プロパナールの製造法

2005
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CHIRAL 6,7-DIHYDROOXEPIN-2(5H)-ONES AND THE AZEPINONE ANALOGUES : CONFORMATION AND DIASTEREOFACIAL SELECTIVITY IN ADDITION TO THE ENONES

1996 Tetrahedron Letters
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Novel 5-Hydroxytryptamine (5-HT3) Receptor Antagonists. Part 1. Synthesis and Structure-Activity Relationships of Conformationally Restricted Fused Imidazole Derivatives.

1996 ChemInform
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Novel 5-Hydroxytryptamine (5-HT3) Receptor Antagonists. Part 2. Synthesis and Structure-Activity Relationships of 4,5,6,7-Tetrahydro- 1H-benzimidazole Derivatives.

1996 ChemInform
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Synthesis of Chiral Cyclic Nitrones via a Nitrosoketene Intermediate and Their Use for the Complete EPC Synthesis of Nonproteinogenic Amino Acids.

1996 ChemInform
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Conjugate addition of 2-trifluoromethyl-1,3-dioxin-4-ones–π-facial selectivity

1996 Chemical Communications
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Use of 1,3-Dioxin-4-ones and Related Compounds in Synthesis. Part 45. 6-Methyl-3-benzylidene-5,6-dihydropyran-2,4-diones: Synthesis and Diastereoselectivity.

1995 ChemInform
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