The role of base ion-pairing in bimolecular elimination : effect of base concentration of the steric couse
- 1 January 1972
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 13 (1) , 23-26
- https://doi.org/10.1016/s0040-4039(01)84228-3
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Stereochemical studies. LIII. Steric course of cycloalkyl 'onium base eliminations: Direct evidence for the syn-anti elimination dichotomy using deuterium labelled cyclodecyl derivativesCollection of Czechoslovak Chemical Communications, 1968
- Stereochemical studies. XLVIII. Effect of base and solvent on the steric course and mechanism of cycloalkene formation in 'onium salt eliminationsCollection of Czechoslovak Chemical Communications, 1968
- Stereochemical studies. L. The mechanism of bimolecular elimination of cycloalkyl tosylates. The scope of syn-elimination: Dependence on reaction conditions and substrate structureCollection of Czechoslovak Chemical Communications, 1968
- Stereochemical studies. IL. The mechanism of cycloalkene formation from cycloalkyl bromides. The scope of the syn-anti bimolecular elimination dichotomyCollection of Czechoslovak Chemical Communications, 1968
- Stereochemical studies. XLI. Solvolysis of cyclodecyl tosylates: Steric course of the reaction and conformational analysisCollection of Czechoslovak Chemical Communications, 1967
- Mechanistic studies in strongly basic media. Part II. Indicator equilibria in t-butyl alcoholJournal of the Chemical Society B: Physical Organic, 1966