Leo R. Fedor

Nucleophilic micelles. II. Effect on the rate of solvolysis of neutral, positively, and negatively charged esters of varied chain length when incorporated into nonfunctional and functional micelles of neutral, positive, and negative charge

Thomas C. Bruice, J. Katzhendler, Leo R. Fedor · Journal of the American Chemical Society · 1968 · 53 citations

Macromolecular Science, Engineering, Macromolecular Engineering +15

Nucleophilic Displacement Reactions at the Thiol Ester Bond. IV. General Base Catalyzed Hydrolysis of Ethyl Trifluorothiolacetate. Kinetic Evidence for the Formation of a Tetrahedral Intermediate¹

Leo R. Fedor, Thomas C. Bruice · Journal of the American Chemical Society · 1965 · 50 citations

Nucleophilic Displacement Reactions, Engineering, Chemical Transformation +13

Base-catalyzed .beta.-elimination reactions in aqueous solution. V. Elimination from 4-(p-substituted-phenoxy)-2-butanones

Leo R. Fedor, W. R. Glave · Journal of the American Chemical Society · 1971 · 35 citations

Engineering, Chemical Analysis, Altmetric Attention Score +18

Nucleophilic Displacement Reactions at the Thiolester Bond. III.¹ Kinetic Demonstration of Metastable Intermediates in the Hydroxylaminolysis and Methoxylaminolysis of Thiolesters and Thiolactones in Aqueous Solutions

Thomas C. Bruice, Leo R. Fedor · Journal of the American Chemical Society · 1964 · 27 citations

Molecular Sciences, Nucleophilic Displacement Reactions, Engineering +15

Base-catalyzed .beta.-elimination reactions in aqueous solution. IV. Elimination from 4-(4-substituted benzoyloxy)-2-butanones

R.C. Cavestri, Leo R. Fedor · Journal of the American Chemical Society · 1970 · 21 citations

Chemical Engineering, Derivative (Chemistry), Engineering +13