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Particle size measurements and scanning electron microscopy (SEM) of cocoa particles refined/conched by conical and cylindrical roller stone melangers

Journal of food engineering, 2017-11, Vol.212, p.146-153

2017

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A new and efficient preparation of 2-aminothiazole-5-carbamides: applications to the synthesis of the anti-cancer drug dasatinib

ARKIVOC, 2010-01, Vol.2010 (6), p.32-38

2010

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Identification and Characterization of Compounds That Potentiate NT-3-Mediated Trk Receptor Activity

Molecular pharmacology, 2006-04, Vol.69 (4), p.1396-1404

2006

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Preparation of Monofluorophenols via the Reaction of Difluorobenzene Derivatives with Potassium Trimethylsilanoate

Synlett, 2009-03, Vol.2009 (4), p.633-637

2009

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Palladium acetate catalyzed cyanation of aryl halides using Buchwald’s 2-(di-t-butylphosphino)-1,1’-binaphthyl

ARKIVOC, 2009-12, Vol.2010 (6), p.47-52

2009

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Discovery of a Fluoroindolo[2,3-a]carbazole Clinical Candidate with Broad Spectrum Antitumor Activity in Preclinical Tumor Models Superior to the Marketed Oncology Drug, CPT-11

Journal of medicinal chemistry, 2005-04, Vol.48 (7), p.2258-2261

2005

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Sordaricin antifungal agents

Bioorganic & medicinal chemistry letters, 2003-02, Vol.13 (3), p.519-524

2003

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Improved procedure for the preparation of 7-methoxy-2-methyl-1-(2-morpholinoethyl)-1H-indole-3-carboxylic acid, key intermediate in the synthesis of novel 3-amidoindole and indolopyridone cannabinoid ligands

ARKIVOC, 2010-01, Vol.2010 (6), p.89-95

2010

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Design and Synthesis of a Fluoroindolocarbazole Series as Selective Topoisomerase I Active Agents. Discovery of Water-Soluble 3,9-Difluoro-12,13-dihydro-13-[6-amino-β- d-glucopyranosyl]-5H,13H-benzo[b]- thienyl[2,3-a]pyrrolo[3,4-c]carbazole- 5,7(6H)-dione (BMS-251873) with Curative Antitumor Activity against Prostate Carcinoma Xenograft Tumor Model

Journal of medicinal chemistry, 2004-03, Vol.47 (7), p.1609-1612

2004

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Carbon-14 labeled methyl 2-chloro-2-oxoacetate: a convenient carbon-14 labeled oxalyl chloride equivalent

Journal of labelled compounds & radiopharmaceuticals, 2009-11, Vol.52 (13), p.549-552

2009

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Novel fluoro-substituted camptothecins : in vivo antitumor activity, reduced gastrointestinal toxicity and pharmacokinetic characterization

Cancer chemotherapy and pharmacology, 2006-07, Vol.58 (1), p.73-85

2006

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Oxime derivatives of sordaricin as potent antifungal agents

Bioorganic & medicinal chemistry letters, 2002-03, Vol.12 (6), p.943-946

2002

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Sordarin Oxazepine Derivatives as Potent Antifungal Agents

Bioorganic & medicinal chemistry letters, 2002-10, Vol.12 (19), p.2757-2760

2002

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A new efficient synthesis of N-(2-(2-(3-methoxy-4-(oxazol-5-yl)phenylamino)oxazol-5-yl)phenyl)-N-methyl-2-morpholinoacetamide (BMS-337197), A novel IMPDH inhibitor

ARKIVOC, 2007-03, Vol.2007 (12), p.36-42

2007

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Synthesis and characterization of tritium labeled N -(( R )-1-(( S )-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl)-3-methyl-1-oxobutan-2-yl)-3-sulfamoylbenzamide: Tritium Labeling and Characterization of a CCR1 Antagonist

Journal of labelled compounds & radiopharmaceuticals, 2015-08, Vol.58 (10), p.414-418

2015

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Non-camptothecin topoisomerase I active compounds as potential anticancer agents

Expert opinion on therapeutic patents, 2000-05, Vol.10 (5), p.635-666

2000

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Synthesis of Biologically Active Piperidine Metabolites of Clopidogrel: Determination of Structure and Analyte Development

Journal of organic chemistry, 2015-07, Vol.80 (14), p.7019-7032

2015

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A New Efficient Synthesis of 5-Aryloxazoles from Arylidene Diacetates and Application to the Preparation of BMS-337197, a Novel IMPDH Inhibitor

Heterocycles, 2006, Vol.68 (1), p.167

2006

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Identification of a broad-Spectrum azasordarin with improved pharmacokinetic properties

Bioorganic & medicinal chemistry letters, 2003-04, Vol.13 (8), p.1419-1423

2003

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Core-modified sordaricin derivatives: Synthesis and antifungal activity

Bioorganic & medicinal chemistry letters, 2002-12, Vol.12 (23), p.3403-3405

2002

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Design and Synthesis of a Fluoroindolocarbazole Series as Selective Topoisomerase I Active Agents. Discovery of Water-Soluble 3,9-Difluoro-12,13-dihydro-13-[6-amino-β-d-glucopyranosyl]-5H,13H-benzo[b]thienyl[2,3-a]pyrrolo[3,4-c]carbazole-5,7(6H)-dione (BMS-251873) with Curative Antitumor Activity against Prostate Carcinoma Xenograft Tumor Model

Journal of medicinal chemistry, 2005-01, Vol.48 (2), p.654-654

2005

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Mild deprotection of 2-(trimethylsilyl)ethyl esters

Tetrahedron letters, 2001-12, Vol.42 (49), p.8593-8595

2001

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Synthesis and characterization of tritium labeled N-((R)-1-((S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl)-3-methyl-1-oxobutan-2-yl)-3-sulfamoylbenzamide

Journal of labelled compounds & radiopharmaceuticals, 2015-08, Vol.58 (10), p.414-418

2015

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Correction to “Synthesis of Biologically Active Piperidine Metabolites of Clopidogrel: Determination of Structure and Analyte Development”

Journal of organic chemistry, 2015-09, Vol.80 (18), p.9370-9370

2015

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Particle size measurements and scanning electron microscopy (SEM) of cocoa particles refined/conched by conical and cylindrical roller stone melangers

A new and efficient preparation of 2-aminothiazole-5-carbamides: applications to the synthesis of the anti-cancer drug dasatinib

Identification and Characterization of Compounds That Potentiate NT-3-Mediated Trk Receptor Activity

Preparation of Monofluorophenols via the Reaction of Difluorobenzene Derivatives with Potassium Trimethylsilanoate

Palladium acetate catalyzed cyanation of aryl halides using Buchwald’s 2-(di-t-butylphosphino)-1,1’-binaphthyl

Discovery of a Fluoroindolo[2,3-a]carbazole Clinical Candidate with Broad Spectrum Antitumor Activity in Preclinical Tumor Models Superior to the Marketed Oncology Drug, CPT-11

Sordaricin antifungal agents

Improved procedure for the preparation of 7-methoxy-2-methyl-1-(2-morpholinoethyl)-1H-indole-3-carboxylic acid, key intermediate in the synthesis of novel 3-amidoindole and indolopyridone cannabinoid ligands

Carbon-14 labeled methyl 2-chloro-2-oxoacetate: a convenient carbon-14 labeled oxalyl chloride equivalent

Novel fluoro-substituted camptothecins : in vivo antitumor activity, reduced gastrointestinal toxicity and pharmacokinetic characterization

Oxime derivatives of sordaricin as potent antifungal agents

Sordarin Oxazepine Derivatives as Potent Antifungal Agents

A new efficient synthesis of N-(2-(2-(3-methoxy-4-(oxazol-5-yl)phenylamino)oxazol-5-yl)phenyl)-N-methyl-2-morpholinoacetamide (BMS-337197), A novel IMPDH inhibitor

Synthesis and characterization of tritium labeled N -(( R )-1-(( S )-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl)-3-methyl-1-oxobutan-2-yl)-3-sulfamoylbenzamide: Tritium Labeling and Characterization of a CCR1 Antagonist

Non-camptothecin topoisomerase I active compounds as potential anticancer agents

Synthesis of Biologically Active Piperidine Metabolites of Clopidogrel: Determination of Structure and Analyte Development

A New Efficient Synthesis of 5-Aryloxazoles from Arylidene Diacetates and Application to the Preparation of BMS-337197, a Novel IMPDH Inhibitor

Identification of a broad-Spectrum azasordarin with improved pharmacokinetic properties

Core-modified sordaricin derivatives: Synthesis and antifungal activity

Mild deprotection of 2-(trimethylsilyl)ethyl esters

Synthesis and characterization of tritium labeled N-((R)-1-((S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl)-3-methyl-1-oxobutan-2-yl)-3-sulfamoylbenzamide

Discovery of a 1H-Benzoimidazol-2-yl)-1H-pyridin-2-one (BMS-536924) Inhibitor of Insulin-like Growth Factor I Receptor Kinase with in Vivo Antitumor Activity

Correction to “Synthesis of Biologically Active Piperidine Metabolites of Clopidogrel: Determination of Structure and Analyte Development”

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