Attenuation of α- and β-methyl effects in the bromination of mono-olefins with conjugatively electron-donating substituents.
- 31 December 1970
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 11 (51) , 4485-4488
- https://doi.org/10.1016/s0040-4039(01)83956-3
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Stable carbonium ions. XCII. Carbon-13 nuclear magnetic resonance spectroscopic study of neighboring halogen participation and substituent effects in carbonium ions. Comparison of substituted cumyl and .beta.-bromocumyl cationsJournal of the American Chemical Society, 1969
- The relationship between isotope effects and reactivityJournal of the American Chemical Society, 1968
- Polar additions to olefins and acetylenes. VI. Nonstereospecific addition of bromine to 1-phenylpropene and trans-anetholeJournal of the American Chemical Society, 1968
- Broensted .alpha. and isotope effects for vinyl ether hydrolysisThe Journal of Physical Chemistry, 1968
- Structure and Reactivity of α,β-Unsaturated Ethers. IV. The Effects of Ring Substituents on the Acid-Catalyzed Hydrolysis Rate of Phenyl Vinyl EtherBulletin of the Chemical Society of Japan, 1968
- Utilisation des effets isotopiques cinetiques en milieu aqueux deutere pour l'etude du mecanisme d'hydratation des α-methylstyrenesTetrahedron Letters, 1967
- 1247. Hydrogen isotope effects in olefin hydration. The relationship of isotope effects to the mechanism of proton transfer from the hydronium ionJournal of the Chemical Society, 1965
- Utilisation d'une méthode “couloampérométrique“ pour l'étude cine̋tique de réactions rapidesJournal of Electroanalytical Chemistry (1959), 1964
- 34. Kinetics of the bromination of some aromatic aminesJournal of the Chemical Society, 1958