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Transition-state modeling of the aldol reaction of boron enolates: a force field approach
National licenceAmerican Chemical Society | 1990| -
Origins of stereoselectivity in chiral boron enolate aldol reactions: A computational study using transition state modellings
National licenceElsevier | 1990| -
Substituted Indole-2-carboxylates as in Vivo Potent Antagonists Acting as the Strychnine-Insensitive Glycine Binding Site
American Chemical Society | 1997| -
Synthesis and Pharmacological Characterization of Novel Druglike Corticotropin-Releasing Factor 1 Antagonists
American Chemical Society | 2008| -
Synthesis and SAR of New 5-Phenyl-3-ureido-1,5-benzodiazepines as Cholecystokinin-B Receptor Antagonists
American Chemical Society | 2000| -
Synthesis and SAR of New 5-Phenyl-3-ureido-1,5-benzodiazepines as Cholecystokinin-B Receptor Antagonists.
American Chemical Society | 2000| -
Sulfonylureido thiazoles as fructose-1,6-bisphosphatase inhibitors for the treatment of Type-2 diabetes
Online Contents | 2010|Contributors: Capelli, Anna M. -
Dihydropyrrole[2,3-d]pyridine Derivatives as Novel Corticotropin-Releasing Factor-1 Antagonists: Mapping of the Receptor Binding Pocket by in Silico Docking Studies
Online Contents | 2008|Contributors: Capelli, Anna M. -
Additions and Corrections - Synthesis and SAR of New 5-Phenyl-3-ureido-1,5-benzodiazepines as Cholecystokinin-B Receptor Antagonists
Online Contents | 2000|Contributors: Capelli, Anna M. -
Articles - Synthesis and SAR of New 5-Phenyl-3-ureido-1,5-benzodiazepines as Cholecystokinin-B Receptor Antagonists
Online Contents | 2000|Contributors: Capelli, Anna M. -
Substituted Indole-2-carboxylates as in Vivo Potent Antagonists Acting as the Strychnine-Insensitive Glycine Binding Site
Online Contents | 1997|Contributors: Capelli, Anna M.
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