The novel orientation in the fluoride promoted elimination reactions. The effect of the various base systems upon the orientation of the base-catalyzed olefin formation.
- 1 January 1970
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 11 (31) , 2727-2728
- https://doi.org/10.1016/s0040-4039(01)98323-6
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
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- Kinetics of reactions of 2-hexyl halides and 2-hexyl p-bromobenzenesulfonate with sodium methoxide in methanol. Evidence that orientation of olefin-forming elimination is not determined by the steric requirements of halogen leaving groupsJournal of the American Chemical Society, 1968
- Steric Effects in Elimination Reactions. XI. The Reaction of Potassium t-Butoxide with 2-Butyl and t-Amyl Halides. The Effect of the Halogen on the Direction of Elimination1Journal of the American Chemical Society, 1966
- Mechanisms of Elimination Reactions. VI. The Effect of the Leaving Group on Orientation in E2 Reactions1,2Journal of the American Chemical Society, 1965