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Which Factors Control the Nucleophilic Reactivities of Enamines?Solvation Accounts for the Counterintuitive Nucleophilicity Ordering of Peroxide Anions.Quantification and Theoretical Analysis of the Electrophilicities of Michael Acceptors.Nucleophilic Reactivities of Bleach ReagentsAmbident Reactivity of Phenolate Anions Revisited: A Quantitative Approach to Phenolate ReactivitiesKinetics and Mechanism of Oxirane Formation by Darzens Condensation of Ketones: Quantification of the Electrophilicities of KetonesElectrophilic Reactivities of Vinyl p-Quinone MethidesLewis Acidity Scale of Diaryliodonium Ions toward Oxygen, Nitrogen, and Halogen Lewis BasesNucleophilicity of Glutathione: A Link to Michael Acceptor ReactivitiesKinetics of Electrophilic Fluorinations of Enamines and Carbanions: Comparison of the Fluorinating Power of N-F ReagentsBasicities and Nucleophilicities of Pyrrolidines and Imidazolidinones Used as OrganocatalystsNucleophilicity and Electrophilicity Parameters for Predicting Absolute Rate Constants of Highly Asynchronous 1,3-Dipolar Cycloadditions of AryldiazomethanesFrom Carbodiimides to Carbon Dioxide: Quantification of the Electrophilic Reactivities of Heteroallenes
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description
researcher
@en
wetenschapper
@nl
name
Armin R Ofial
@en
Armin R Ofial
@nl
type
label
Armin R Ofial
@en
Armin R Ofial
@nl
prefLabel
Armin R Ofial
@en
Armin R Ofial
@nl
P31
P496
0000-0002-9600-2793