M. Ruasse

发表

Hydrogen peroxide oxidation of mustard-model sulfides catalyzed by iron and manganese tetraarylporphyrines. Oxygen transfer to sulfides versus H(2)O(2) dismutation and catalyst breakdown.

M. Marín, A. Marques, M. Ruasse, 2001, The Journal of organic chemistry.

Couloamperometry, a high-performance stationary technique for following very fast reactions

J. Dubois, M. Ruasse, D. Poupard, 1983 .

Glossary of terms used in physical organic chemistry (IUPAC Recommendations 2021)

L. Radom, C. Perrin, P. Fernandes, 2022, Pure and Applied Chemistry.

Self-association mechanisms in aqueous media: dimerization versus micellization of alkyl-ellipticinium derivatives

A. Adenier, Marie-Anne Cordonnier, M. Schwaller, 1993 .

Kinetics and mechanisms of the reactions of benzoyl derivatives of nucleophiles: dependence of the solvation requirement of the reaction on the structures of the nucleophile and the acyl group

O. E. Seoud, M. Ruasse, Monica S. Ferreira, 2005 .

Remarkable efficiency of iron(III) versus manganese(III) tetraphenylporphyrins as catalysts for fast and quantitative oxidation of sulfides into sulfones by hydrogen peroxide

M. D. Matteo, A. Marques, M. Ruasse, 1998 .

Couloamperometry. A fast kinetic technique for halogenations. I. Bromination rate constants of highly reactive enol ethers

J. Dubois, M. Ruasse, D. Poupard, 1983 .

Solvation and steric effects on electrophilic reactivity of ethylenic compounds. Part 4. Bromination of oct-1-ene in anionic microemulsions

S. Krys, I. Blagoeva, M. Ruasse, 1993 .

Electrophilic Additions to Dienes and Polyenes

C. Chiappe, M. Ruasse, 2001 .

Changes in the relative contribution of specific and general base catalysis in cationic micelles. The cyclization of substituted ethyl hydantoates.

I. Blagoeva, M. Toteva, M. Ruasse, 2001, The Journal of organic chemistry.

Electrophilic Bromination of Carbon—Carbon Double Bonds: Structure, Solvent and Mechanism

M. Ruasse, 1993 .

Bromonium ions or .beta.-bromocarbocations in olefin bromination. A kinetic approach to product selectivities

M. Ruasse, 1990 .

Intermediaires aryl carbonium en bromation. Nivellement de la contribution d'un cycle aromatique par les substituants donneurs de l'ion carbonium ArC+(R′)R″

J. Dubois, M. Ruasse, A. Argile, 1975 .

Solvation and steric effects on electrophilic reactivity of ethylenic compounds. 2. Kinetic criteria for nucleophilic assistance and return in bromination

M. Ruasse, S. Motallebi, B. Galland, 1991 .

pH‐independent hydrolysis of 4‐nitrophenyl 2,2‐dichloropropionate in aqueous micellar solutions: relative contributions of hydrophobic and electrostatic interactions

M. Ruasse, S. Possidonio, Omar A. Ei Seoud, 2001 .

Electrophilic Additions to Highly Reactive Enol Ethers. The Particular Role of Resonance in Determining the Kinetic Selectivity Evidenced by Extensive Comparison of Olefin Bromination and Hydration

M. Ruasse, 1985 .

Preassociation, Free-Ion, and Ion-Pair Pathways in the Electrophilic Bromination of Substituted cis- and trans-Stilbenes in Protic Solvents

G. Bellucci, R. Bianchini, M. Ruasse, 1997 .

Interfacial ion exchange between monovalent and divalent anions in cationic micelles, revised in the light of correlation analysis

I. Blagoeva, M. Ruasse, N. Ouarti, 2005 .

Optimization of micellar catalysis of nucleophilic substitution reactions in buffered solutions of cetyltrimethylammonium halide surfactants, part 2: buffers in the pH range 7–8

I. Blagoeva, M. Ruasse, N. Ouarti, 2001 .

NUCLEOPHILIC SUBSTITUTION AT SULFONYL SULFUR ATOM: AMINOLYSIS OF 1-TOSYL-3-METHYLIMIDAZOLIUM CHLORIDE IN AQUEOUS MEDIUM

M. Ruasse, P. Monjoint, 1984 .

Nucleophilic substitution at sulfonyl sulfur atom: Aminolysis of 1-tosyl-3-methyl imidazolium chloride in aqueous medium.

M. Ruasse, P. Monjoint, 1984 .

Sulphonyl transfer reactions

H. Maskill, M. Ruasse, I. Gordon, 1989 .

ROLE OF THE SOLVENT IN BROMINE ADDITIONS TO OLEFINS, SOLVENT INDEPENDENCE OF THE CHARGE DISTRIBUTION IN TRANSITION STATES AND INTERMEDIATES

J. Dubois, M. Ruasse, 1975 .

An amperometric method for the determination of very low halogen concentrations in protic media

J. Dubois, M. Ruasse, D. Poupard, 1983 .

An Ion-Exchange Reaction as Measured by Surface-Enhanced Raman Spectroscopy on Silver Colloids

J. Aubard, E. Wentrup-Byrne, J. Pantigny, 1995 .

Methyl effect in electrophilic additions. An open carbonium ion-like rate-determining transition state for the bromination of styrene

J. Dubois, M. Ruasse, A. Argile, 1979 .

Styrene bromination. The competition between carbonium and bromonium ion pathways evidenced by increasing the electronic demand on the bromine atom.

J. Dubois, M. Ruasse, A. Argile, 1978 .

Kinetics and mechanism of phosphate-catalyzed hydrolysis of benzoate esters: comparison with nucleophilic catalysis by imidazole and o-iodosobenzoate

M. Ruasse, W. A. Rodrigues, O. A. Seoud, 2002 .

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

J. Dubois, M. Ruasse, 1975 .

An MNDO approach to the symmetry of bromine bridging in substituted bromonium ions

M. Ruasse, E. Evleth, B. Galland, 1990 .

Stereo-, Regio- and Chemoselectivity of Bromination of Ethylenic Compounds

M. Ruasse, 2010 .

Solvation and steric effects on electrophilic reactivity of ethylenic compounds. 1. Stereochemistry and bromination of congested adamantylidenealkanes

J. Lomas, M. Ruasse, S. Motallebi, 1990 .

Kinetic study of the fast halogen-trihalide ion equilibria in protic media by the Raman-laser temperature-jump technique. A non-diffusion-controlled ion-molecule reaction

J. Aubard, A. Adenier, M. Ruasse, 1986 .

The nucleophilic contribution of the solvent in olefin bromination. II. Reactivity dependence of the nucleophilic solvation in bromination via .beta.-bromocarbocations

M. Ruasse, E. Lefebvre, 1984 .

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

M. Ruasse, Ben-Li Zhang, 1984 .

BROMOVINYL CATIONS IN BROMINATION. SIMILARITY OF SOLVENT EFFECTS IN LIMITING SOLVOLYSIS AND IN BROMINATION OF OLEFINS AND ACETYLENES

J. Dubois, M. Ruasse, 1977 .

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

J. Dubois, M. Ruasse, A. Argile, 1984 .

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

J. Dubois, M. Ruasse, A. Argile, 1984 .

Nucleophilic Reactivity of the CTACl-Micelle-Bound Fluoride Ion: The Influence of Water Concentration and Ionic Strength at the Micellar Interface

I. Blagoeva, M. Ruasse, Priscilla L. Silva, 2003 .

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

J. Dubois, M. Ruasse, 1973 .

Interactive free energy relationships for nonadditive multiple substituent effects. Cross-interaction constant in .alpha.-methylstilbene bromination

M. Ruasse, A. Argile, 1983 .

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

M. Ruasse, A. Argile, 1983 .

Reactivity of ethylenic compounds. 42. The multipathway mechanism in styrene bromination: competition between bromonium and carbonium ion intermediates

J. Dubois, M. Ruasse, A. Argile, 1978 .

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

J. Dubois, M. Ruasse, 1974 .

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

J. Dubois, M. Ruasse, 1972 .

The polar reaction constant for alkene chlorination. similarity and differences in the chloronium and bromonium ion like transition states.

J. Dubois, M. Ruasse, E. Bienvenue-Goetz, 1982 .

Competitive formation of secondary and tertiary aryl bromocarbonium ions in bromination.

J. Dubois, M. Ruasse, A. Argile, 1976 .

Optimization of Micellar Catalysis of Nucleophilic Substitutions in Buffered Cetyltrimethylammonium Salt Solutions. 1. Buffers for the 9−10 pH Range†

A. Marques, M. Ruasse, N. Ouarti, 2000 .

Bromination of stilbenes. Non-linear free energy relationship

J. Dubois, M. Ruasse, 1970 .

Organic reactions in micro-organized media: Why and how?

Luis García-Río, Antonio Marques, J. Mejuto, 1997 .

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

D. Lenoir, C. Pomelli, C. Chiappe, 2003, Journal of the American Chemical Society.

Reactivities of methylenetriangulanes and spirocyclopropanated bicyclopropylidenes toward bromine. Relative stabilities of spirocyclopropanated versus methyl-substituted bromonium ions.

A. de Meijere, Th Späth, Y. Apeloig, 2002, The Journal of organic chemistry.