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Characterization of Orally Active Nonpeptide Vasopressin V2 Receptor Agonist. Synthesis and Biological Evaluation of Both the (5R)- and (5S)-Enantioisomers of 2-[1-(2-Chloro-4-pyrrolidin-1-yl-benzoyl)-2,3,4,5-tetrahydro-1H-1-benzazepin- 5-yl]-N-isopropylacetamide

Journal of medicinal chemistry, 2002-08, Vol.45 (17), p.3805-3808

2002

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Pipe-shaped BiCS flash memory with 16 stacked layers and multi-level-cell operation for ultra high density storage devices

2009 Symposium on VLSI Technology, 2009, p.136-137

2009

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Optimal Integration and Characteristics of Vertical Array Devices for Ultra-High Density, Bit-Cost Scalable Flash Memory

2007 IEEE International Electron Devices Meeting, 2007, p.449-452

2007

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Studies on total syntheses of antitumor styryllactones: Stereoselective total syntheses of (+)-goniofufurone, (+)-goniobutenolide A, and (−)-goniobutenolide B

Tetrahedron, 1996-05, Vol.52 (19), p.6547-6560

1996

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Enantioselective Synthesis of the Metabolites of Vasopressin V2 Receptor Antagonist OPC-31260 via Lipase-Catalyzed Transesterification

Tetrahedron, 2000-06, Vol.56 (27), p.4667-4682

2000

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Stereoselective synthesis of alkenylated malonic diamide using masked acyl cyanide

Tetrahedron letters, 1999-02, Vol.40 (7), p.1319-1322

1999

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Synthetic disproof against the structure proposed for alectrol, the germination stimulant from Vigna unguiculata

Tetrahedron letters, 1998-08, Vol.39 (33), p.6023-6026

1998

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Synthesis and determination of the absolute configuration of fudecalone

ARKIVOC, 2003-11, Vol.2003 (8), p.267-282

2003

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Syntheses of (±)- and (+)-Sorgolactone, the Germination Stimulant fromSorghum bicolor

European journal of organic chemistry, 1999-09, Vol.1999 (9), p.2183-2194

1999

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Synthetic Disproof of the Structure Proposed for Alectrol, the Germination Stimulant fromVigna unguiculata

European journal of organic chemistry, 1999-09, Vol.1999 (9), p.2195-2199

1999

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Glochidionolactones A-F : Butenolide Glucosides from Leaves of Glochidion zeylanicum (GAERTN) A. JUSS

Chemical and Pharmaceutical Bulletin, 2000/04/01, Vol.48(4), pp.547-551

2000

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An Efficient Synthesis of Optical Isomers of Vasopressin V2 Receptor Antagonist OPC-41061 by Lipase-catalyzed Enantioselective Transesterification

Heterocycles, 2001, Vol.54 (1), p.131

2001

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Disturbless flash memory due to high boost efficiency on BiCS structure and optimal memory film stack for ultra high density storage device

2008 IEEE International Electron Devices Meeting, 2008, p.1-4

2008

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Synthesis of a sulfulr-containing 10-membered enediyne model compound related to the esperamicin/calicheamicin/dynemicin agylcones

Tetrahedron letters, 1991, Vol.32 (34), p.4363-4366

1991

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Synthetic Studies on Cephalotaxus Alkaloids. A Synthesis of (±)-Cephalotaxine

Chemical and Pharmaceutical Bulletin, 1993/02/15, Vol.41(2), pp.276-281

1993

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The Absolute Configuration of (R)-(+)-Nadifloxacin

Chemical and Pharmaceutical Bulletin, 1996/02/15, Vol.44(2), pp.421-423

1996

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Crystal Structures of Nadifloxacin Anhydride and Its Hemihydrate

Chemical and Pharmaceutical Bulletin, 1994/04/15, Vol.42(4), pp.872-876

1994

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Silicon-carbon unsaturated compounds. 47. Dimerization of silenes generated from 1,4-bis(pentamethyldisilanyl)benzene and 1-(pentamethyldisilanyl)-4-(trimethylsilyl)benzene and the molecular structure of a dimer

Organometallics, 1993-09, Vol.12 (9), p.3474-3479

1993

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A Practical Synthesis of (S)-(-)-Nadifloxacin : Novel Acid-Catalyzed Racemization of Tetrahydroquinaldine Derivative

Chemical and Pharmaceutical Bulletin, 1996/04/15, Vol.44(4), pp.642-645

1996

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Characterization of Orally Active Nonpeptide Vasopressin V 2 Receptor Agonist. Synthesis and Biological Evaluation of Both the (5 R )- and (5 S )-Enantioisomers of 2-[1-(2-Chloro-4-pyrrolidin-1-yl-benzoyl)-2,3,4,5-tetrahydro-1 H -1-benzazepin- 5-yl]- N -isopropylacetamide

Journal of medicinal chemistry, 2002-08, Vol.45 (17), p.3805-3808

2002

Volltextzugriff (PDF)

Structure of an Anti-plasmin Inhibitor, Eckol, Isolated from the Brown Alga Ecklonia kurome OKAMURA and Inhibitory Activities of Its Derivatives on Plasma Plasmin Inhibitors

Chemical and Pharmaceutical Bulletin, 1989/02/25, Vol.37(2), pp.349-353

1989

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An efficient synthesis of pironetins employing a useful chiral building block,(1S,5S,6R)-5-hydroxybicyclo[4.1.0]heptan-2-one

Tetrahedron, 1999-08, Vol.55 (32), p.9755-9776

1999

Volltextzugriff (PDF)

NOVEL INHIBITORS OF SUPEROXIDE ANION GENERATION, OPC-15160 AND OPC-15161: TAXONOMY, FERMENTATION, ISOLATION, PHYSICO-CHEMICAL PROPERTIES, BIOLOGICAL CHARACTERISTICS AND STRUCTURE DETERMINATION

The Journal of Antibiotics, 1991/01/25, Vol.44(1), pp.52-58

1991

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Novel sesquiterpene esters with alkaloid and monoterpene and related compounds from Tripterygium hypoglaucum: A new class of potent anti-HIV agents

Tetrahedron letters, 1999-04, Vol.40 (15), p.2969-2972

1999

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Synthesis of 5-Fluorouracil Derivatives Containing an Inhibitor of 5-Fluorouracil Degradation

Chemical and Pharmaceutical Bulletin, 1993/09/15, Vol.41(9), pp.1498-1506

1993

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Characterization of Orally Active Nonpeptide Vasopressin V2 Receptor Agonist. Synthesis and Biological Evaluation of Both the (5R)- and (5S)-Enantioisomers of 2-[1-(2-Chloro-4-pyrrolidin-1-yl-benzoyl)-2,3,4,5-tetrahydro-1H-1-benzazepin- 5-yl]-N-isopropylacetamide

Pipe-shaped BiCS flash memory with 16 stacked layers and multi-level-cell operation for ultra high density storage devices

Optimal Integration and Characteristics of Vertical Array Devices for Ultra-High Density, Bit-Cost Scalable Flash Memory

Studies on total syntheses of antitumor styryllactones: Stereoselective total syntheses of (+)-goniofufurone, (+)-goniobutenolide A, and (−)-goniobutenolide B

Enantioselective Synthesis of the Metabolites of Vasopressin V2 Receptor Antagonist OPC-31260 via Lipase-Catalyzed Transesterification

Stereoselective synthesis of alkenylated malonic diamide using masked acyl cyanide

Synthetic disproof against the structure proposed for alectrol, the germination stimulant from Vigna unguiculata

Synthesis and determination of the absolute configuration of fudecalone

Syntheses of (±)- and (+)-Sorgolactone, the Germination Stimulant fromSorghum bicolor

Synthetic Disproof of the Structure Proposed for Alectrol, the Germination Stimulant fromVigna unguiculata

Glochidionolactones A-F : Butenolide Glucosides from Leaves of Glochidion zeylanicum (GAERTN) A. JUSS

An Efficient Synthesis of Optical Isomers of Vasopressin V2 Receptor Antagonist OPC-41061 by Lipase-catalyzed Enantioselective Transesterification

Disturbless flash memory due to high boost efficiency on BiCS structure and optimal memory film stack for ultra high density storage device

Synthesis of a sulfulr-containing 10-membered enediyne model compound related to the esperamicin/calicheamicin/dynemicin agylcones

Synthetic Studies on Cephalotaxus Alkaloids. A Synthesis of (±)-Cephalotaxine

The Absolute Configuration of (R)-(+)-Nadifloxacin

Crystal Structures of Nadifloxacin Anhydride and Its Hemihydrate

Silicon-carbon unsaturated compounds. 47. Dimerization of silenes generated from 1,4-bis(pentamethyldisilanyl)benzene and 1-(pentamethyldisilanyl)-4-(trimethylsilyl)benzene and the molecular structure of a dimer

A Practical Synthesis of (S)-(-)-Nadifloxacin : Novel Acid-Catalyzed Racemization of Tetrahydroquinaldine Derivative

Characterization of Orally Active Nonpeptide Vasopressin V 2 Receptor Agonist. Synthesis and Biological Evaluation of Both the (5 R )- and (5 S )-Enantioisomers of 2-[1-(2-Chloro-4-pyrrolidin-1-yl-benzoyl)-2,3,4,5-tetrahydro-1 H -1-benzazepin- 5-yl]- N -isopropylacetamide

Structure of an Anti-plasmin Inhibitor, Eckol, Isolated from the Brown Alga Ecklonia kurome OKAMURA and Inhibitory Activities of Its Derivatives on Plasma Plasmin Inhibitors

An efficient synthesis of pironetins employing a useful chiral building block,(1S,5S,6R)-5-hydroxybicyclo[4.1.0]heptan-2-one

NOVEL INHIBITORS OF SUPEROXIDE ANION GENERATION, OPC-15160 AND OPC-15161: TAXONOMY, FERMENTATION, ISOLATION, PHYSICO-CHEMICAL PROPERTIES, BIOLOGICAL CHARACTERISTICS AND STRUCTURE DETERMINATION

Novel sesquiterpene esters with alkaloid and monoterpene and related compounds from Tripterygium hypoglaucum: A new class of potent anti-HIV agents

Synthesis of 5-Fluorouracil Derivatives Containing an Inhibitor of 5-Fluorouracil Degradation

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