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Reactivity of ethylenic compounds. 42. The multipathway mechanism in styrene bromination: competition between bromonium and carbonium ion intermediates
National licenceAmerican Chemical Society | 1978| -
Methyl effect in electrophilic additions. An open carbonium ion-like rate-determining transition state for the bromination of styrene
National licenceAmerican Chemical Society | 1979| -
An Ion-Exchange Reaction As Measured by Surface-Enhanced Raman Spectroscopy on Silver Colloids
British Library Online Contents | 1995| -
Substituent Dependence of the Diastereofacial Selectivity in Iodination and Bromination of Glycals and Related Cyclic Enol Ethers
British Library Online Contents | 2000| -
Solvation and Steric Effects on Electrophilic Reactivity of Ethylenic Compounds. 3. Stereo-, Regio-, and Chemoselectivity of Alkene Bromination in Methanol
British Library Online Contents | 1993| -
Kinetics and mechanism of phosphate-catalyzed hydrolysis of benzoate esters: comparison with nucleophilic catalysis by imidazole and o-iodosobenzoate
British Library Online Contents | 2002| -
Interfacial ion exchange between monovalent and divalent anions in cationic micelles, revised in the light of correlation analysis
British Library Online Contents | 2005| -
Alkene reactivity. Influence of the entering electrophile and limitations of linear free energy relationships in electrophilic additions
National licenceAmerican Chemical Society | 1979| -
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
British Library Conference Proceedings | 2005|
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