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Synthesis of a Novel Series of Tricyclic Indan Derivatives as Melatonin Receptor Agonists

Journal of medicinal chemistry, 2002-09, Vol.45 (19), p.4222-4239

2002

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Axially Chiral 1,7-Naphthyridine-6-carboxamide Derivatives as Orally Active Tachykinin NK1 Receptor Antagonists: Synthesis, Antagonistic Activity, and Effects on Bladder Functions

Journal of medicinal chemistry, 1999-09, Vol.42 (19), p.3982-3993

1999

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Approach to the stereoselective synthesis of melatonin receptor agonist Ramelteon via asymmetric hydrogenation

Tetrahedron: asymmetry, 2006-01, Vol.17 (2), p.184-190

2006

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Axially Chiral N-Benzyl-N,7-dimethyl-5-phenyl-1,7-naphthyridine-6-carboxamide Derivatives as Tachykinin NK1 Receptor Antagonists: Determination of the Absolute Stereochemical Requirements

Journal of medicinal chemistry, 1998-10, Vol.41 (22), p.4232-4239

1998

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Novel 5-Substituted 2,4-Thiazolidinedione and 2,4-Oxazolidinedione Derivatives as Insulin Sensitizers with Antidiabetic Activities

Journal of medicinal chemistry, 2002-03, Vol.45 (7), p.1518-1534

2002

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Stereoselective Reduction of Ethyl 2-Methyl-3-oxobutanoate by Bacteria

Bioscience, biotechnology, and biochemistry, 1996-01, Vol.60 (1), p.95-98

1996

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The First Example for Cycloenantiomeric Hexahomooxacalix[3]arenes

Chemical and Pharmaceutical Bulletin, 2001, Vol.49(4), pp.507-509

2001

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Purification and Characterization of Ethyl 2-Methyl-3-oxobutanoate Reductase from Klebsiella pneumoniae IF03319

Bioscience, biotechnology, and biochemistry, 1996-01, Vol.60 (5), p.760-764

1996

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Synthesis of a Novel Series of Benzocycloalkene Derivatives as Melatonin Receptor Agonists

Journal of medicinal chemistry, 2002-09, Vol.45 (19), p.4212-4221

2002

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Enantioselective hydrogenation of β-keto esters catalyzed by P-chiral bis(dialkylphosphino)ethanes-Ru(II)

Tetrahedron letters, 1999-03, Vol.40 (13), p.2577-2580

1999

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Enantioselective synthesis of an axially chiral 1,7-naphthyridine-6-carboxamide derivative having potent antagonist activity at the NK1 receptor

Chemical communications (Cambridge, England), 1998 (19), p.2141-2142

1998

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Kinetic Resolution of an Indan Derivative Using Bacillus sp. SUI-12

Journal of bioscience and bioengineering, 2002-01, Vol.93 (1), p.44

2002

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Spirocyclopropane Compounds. VI. : Synthesis of Spiro[benzo[b]-thiophene-2(3H), 1'-cyclopropan]-3-ones

Chemical and Pharmaceutical Bulletin, 1986/05/25, Vol.34(5), pp.1939-1945

1986

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Purification and Characterization of Ethyl 2-Methyl-3-oxobutanoate Reductase from Klebsiella pheumoniae IFO3319

Bioscience, biotechnology, and biochemistry, 1996-05, Vol.60 (5), p.760

1996

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Kinetic resolution of an indan derivative using Bacillus sp. SUI-12: Synthesis of a key intermediate of the melatonin receptor agonist TAK-375

Journal of bioscience and bioengineering, 2002, Vol.93 (1), p.44-47

2002

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Axially Chiral 1,7-Naphthyridine-6-carboxamide Derivatives as Orally Active Tachykinin NK 1 Receptor Antagonists: Synthesis, Antagonistic Activity, and Effects on Bladder Functions

Journal of medicinal chemistry, 1999-09, Vol.42 (19), p.3982-3993

1999

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Axially Chiral N -Benzyl- N ,7-dimethyl-5-phenyl-1,7-naphthyridine-6-carboxamide Derivatives as Tachykinin NK 1 Receptor Antagonists: Determination of the Absolute Stereochemical Requirements

Journal of medicinal chemistry, 1998-10, Vol.41 (22), p.4232-4239

1998

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Spirocyclopropane compounds. V. One-step synthesis of 5-acetylspiro(benzofuran-2(3H),1'-cyclopropan)-3-one

Chemical & pharmaceutical bulletin, 1984, Vol.32 (9), p.3373-3377

1984

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Spirocyclopropane compounds. IV. Synthesis of 5-acetylspiro(benzofuran-2(3H),1'-cyclopropan)-3-one related compounds for evaluation as gastric antisecretory and antiulcer agents

Chemical & pharmaceutical bulletin, 1984, Vol.32 (9), p.3551-3560

1984

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Spirocyclopropane Compounds. I. Synthesis and Reactivity of Spiro [cyclopropane-1, 2'-[2H] indol]-3'(1'H)-ones

Chemical and Pharmaceutical Bulletin, 1981/07/25, Vol.29(7), pp.1900-1911

1981

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Spirocyclopropane compounds. III. Synthesis of spiro(benzofuran-2(3H),1'-cyclopropan)-3-ones for evaluation as gastric antisecretory and antiulcer agents

Chemical & pharmaceutical bulletin, 1984, Vol.32 (9), p.3532-3550

1984

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Neighboring Group Participation in Solvolysis. XIII. Kinetic Isotope Effects in Solvolysis of 2-Arylethyl p-Nitrobenzenesulfonates

Bulletin of the Chemical Society of Japan, 1981, Vol.54 (11), p.3536-3540

1981

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Spirocyclopropane Compounds. II. Synthesis and Biological Activities of Spiro [cyclopropane-1, 2'-[2H] indol]-3'(1'H)-ones

Chemical and Pharmaceutical Bulletin, 1981/07/25, Vol.29(7), pp.1912-1919

1981

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Spirocyclopropane Compounds. VI

Chemical & pharmaceutical bulletin, 1986-05, Vol.34 (5), p.1939

1986

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ChemInform Abstract: The First Example for Cycloenantiomeric Hexahomooxacalix[3]arenes

ChemInform, 2001-09, Vol.32 (39), p.no-no

2001

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Synthesis of a Novel Series of Tricyclic Indan Derivatives as Melatonin Receptor Agonists

Axially Chiral 1,7-Naphthyridine-6-carboxamide Derivatives as Orally Active Tachykinin NK1 Receptor Antagonists: Synthesis, Antagonistic Activity, and Effects on Bladder Functions

Approach to the stereoselective synthesis of melatonin receptor agonist Ramelteon via asymmetric hydrogenation

Axially Chiral N-Benzyl-N,7-dimethyl-5-phenyl-1,7-naphthyridine-6-carboxamide Derivatives as Tachykinin NK1 Receptor Antagonists: Determination of the Absolute Stereochemical Requirements

Novel 5-Substituted 2,4-Thiazolidinedione and 2,4-Oxazolidinedione Derivatives as Insulin Sensitizers with Antidiabetic Activities

Stereoselective Reduction of Ethyl 2-Methyl-3-oxobutanoate by Bacteria

The First Example for Cycloenantiomeric Hexahomooxacalix[3]arenes

Purification and Characterization of Ethyl 2-Methyl-3-oxobutanoate Reductase from Klebsiella pneumoniae IF03319

Synthesis of a Novel Series of Benzocycloalkene Derivatives as Melatonin Receptor Agonists

Enantioselective hydrogenation of β-keto esters catalyzed by P-chiral bis(dialkylphosphino)ethanes-Ru(II)

Enantioselective synthesis of an axially chiral 1,7-naphthyridine-6-carboxamide derivative having potent antagonist activity at the NK1 receptor

Kinetic Resolution of an Indan Derivative Using Bacillus sp. SUI-12

Spirocyclopropane Compounds. VI. : Synthesis of Spiro[benzo[b]-thiophene-2(3H), 1'-cyclopropan]-3-ones

Purification and Characterization of Ethyl 2-Methyl-3-oxobutanoate Reductase from Klebsiella pheumoniae IFO3319

Kinetic resolution of an indan derivative using Bacillus sp. SUI-12: Synthesis of a key intermediate of the melatonin receptor agonist TAK-375

Axially Chiral 1,7-Naphthyridine-6-carboxamide Derivatives as Orally Active Tachykinin NK 1 Receptor Antagonists: Synthesis, Antagonistic Activity, and Effects on Bladder Functions

Axially Chiral N -Benzyl- N ,7-dimethyl-5-phenyl-1,7-naphthyridine-6-carboxamide Derivatives as Tachykinin NK 1 Receptor Antagonists: Determination of the Absolute Stereochemical Requirements

Spirocyclopropane compounds. V. One-step synthesis of 5-acetylspiro(benzofuran-2(3H),1'-cyclopropan)-3-one

Spirocyclopropane compounds. IV. Synthesis of 5-acetylspiro(benzofuran-2(3H),1'-cyclopropan)-3-one related compounds for evaluation as gastric antisecretory and antiulcer agents

Spirocyclopropane Compounds. I. Synthesis and Reactivity of Spiro [cyclopropane-1, 2'-[2H] indol]-3'(1'H)-ones

Spirocyclopropane compounds. III. Synthesis of spiro(benzofuran-2(3H),1'-cyclopropan)-3-ones for evaluation as gastric antisecretory and antiulcer agents

Neighboring Group Participation in Solvolysis. XIII. Kinetic Isotope Effects in Solvolysis of 2-Arylethyl p-Nitrobenzenesulfonates

Spirocyclopropane Compounds. II. Synthesis and Biological Activities of Spiro [cyclopropane-1, 2'-[2H] indol]-3'(1'H)-ones

Spirocyclopropane Compounds. VI

ChemInform Abstract: The First Example for Cycloenantiomeric Hexahomooxacalix[3]arenes

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