Marie Francoise Ruasse

Theoretical and experimental evaluation of IFER for MSE (interactive free energy relationship for multiple-substituent effects): Mechanistic significance of the reaction constant and cross-interaction constant

Substituent dependence of the diastereofacial selectivity in iodination and bromination of glycals and related cyclic enol ethers

Role of the solvent in bromine additions to olefins. Solvent independence of the charge distribution in transition states and intermediates

Reactivity of ethylenic compounds. Bromination. XXX. Electrophilic bromination of aromatic conjugated olefins. I. Evaluation of a competitive path mechanism in bromination of trans monosubstituted stilbenes

Electrophilic bromination of aromatic conjugated olefins. II. Mechanism of the dual-path additions in stilbene bromination. Evidence from multiple substituent effects for carbonium ion intermediates

Polarizability effects and dispersion interactions in alkene-Br2 pi-complexes.

Multipathway bromination of stilbenes. Competition between carbonium and bromonium ion intermediates

Multipathway mechanism in arylolefin bromination: competition between tertiary and secondary carbocation pathways

Selectivity relationships and substituent-substituent interactions in carbocation-forming bromination. The transition-state contribution to the .rho. variation

The nucleophilic contribution of the solvent in olefin bromination. I. Steric inhibition to nucleophilic solvation in alkene bromination via brominium ions