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The <i>syn</i> and <i>anti</i> Steric Course in Bimolecular Olefin‐Forming Eliminations
94
Citations
60
References
1972
Year
Anti Steric CourseEngineeringAlkene MetathesisBiochemistryNatural SciencesOrganic ChemistryOnium BasesOrganometallic CatalysisBimolecular Olefin‐forming EliminationsStereoselective SynthesisChemistrySupramolecular ChemistryAsymmetric CatalysisSynthetic ChemistryBiomolecular Engineering
Abstract Earlier evidence led to the view that in bimolecular olefin‐forming eliminations the anti steric course is generally preferred over the syn. Recent experiments, however, show that in some common bimolecular elimination reactions, notably those involving onium bases, syn‐ and anti‐eliminations proceed side by side, the former preferentially leading to the trans‐ and the latter to the cis‐olefins.
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