The Effect of Solvent Variation on Nucleophilic Substitution Rates of Methyl Tosylate
- 1 November 1972
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 55 (7) , 2400-2406
- https://doi.org/10.1002/hlca.19720550714
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Nucleophile Substitution von Methyltosylat in dipolar aprotischen LösungsmittelnHelvetica Chimica Acta, 1971
- Ion-pair Reactivity in Isotopic Exchange Reactions. III. Ion-pairs of Tetraalkyl Ammonium Halides.Acta Chemica Scandinavica, 1970
- Ion-Pair Reactivity in Isotopic Exchange Reactions. II. Lithium Bromide in Acetone as Solvent.Acta Chemica Scandinavica, 1970
- Protic-dipolar aprotic solvent effects on rates of bimolecular reactionsChemical Reviews, 1969
- Solvation enthalpies and rates of nucleophilic displacement of alkali halides in dimethyl sulfoxideJournal of the American Chemical Society, 1968
- Solvation of ions. XIV. Protic-dipolar aprotic solvent effects on rates of bimolecular reactions. Solvent activity coefficients of reactants and transition states at 25°.Journal of the American Chemical Society, 1968
- Conductance of Electrolytes in Anhydrous AcetoneJournal of the American Chemical Society, 1966
- The SN Mechanism in Aromatic Compounds. Part XXVII.1 A Quantitative Approach to Aromatic Nucleophilic SubstitutionJournal of the American Chemical Society, 1963
- The effects of solvation on the properties of anions in dipolar aprotic solventsQuarterly Reviews, Chemical Society, 1962
- Dipolar Aprotic Solvents in Bimolecular Aromatic Nucleophilic Substitution Reactions1Journal of the American Chemical Society, 1961