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Robert M. Pratt

National Institutes of Health

104

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Targeting conserved water molecules: design of 4-aryl-5-cyanopyrrolo[2,3-d]pyrimidine Hsp90 inhibitors using fragment-based screening and structure-based optimization.

2012 Bioorganic & Medicinal Chemistry
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Fatty acid amide hydrolase inhibitors. Surprising selectivity of chiral azetidine ureas.

2009 Bioorganic & Medicinal Chemistry Letters
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Antagonists of the human adenosine A2A receptor. Part 1: Discovery and synthesis of thieno[3,2-d]pyrimidine-4-methanone derivatives

2008 Bioorganic & Medicinal Chemistry Letters
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Antagonists of the human adenosine A2A receptor. Part 2: Design and synthesis of 4-arylthieno[3,2-d]pyrimidine derivatives

2008 Bioorganic & Medicinal Chemistry Letters
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Antagonists of the human adenosine A2A receptor. Part 3 Design and synthesis of pyrazolo[3,4-d]pyrimidines, pyrrolo[2,3-d]pyrimidines and 6-arylpurines

2008 Bioorganic & Medicinal Chemistry Letters
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Radion Reactions To Form Vinylphosphonothioates

2005 Synlett
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-azetidinecarboxamide derivatives for use for treatment of CB1 receptor-mediated diseases

2004
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Derives d'azetidinecarboxamide et leur utilisation dans le traitement de troubles medies par les recepteur cb1

2004
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Use of a Modified Leimgruber–Batcho Reaction to Prepare 6‐Chloro‐5‐fluoroindole

2004 Synthetic Communications
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Use of a Modified Leimgruber–Batcho Reaction to Prepare 6‐Chloro‐5‐fluoroindole

2004 Synthetic Communications
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