Publication | Closed Access
An Easy Procedure for the Highly Regioselective Conversion of Epoxides to Halohydrins
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Citations
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References
1992
Year
HalogenationEngineeringAlkene MetathesisBiochemistryNatural SciencesEasy ProcedureHighly Regioselective ConversionLithium HalidesCorresponding HalohydrinsOrganic ChemistryCatalysisEpoxy AlcoholsChemistryStereoselective SynthesisNatural Product SynthesisEnantioselective SynthesisBiomolecular Engineering
Abstract several epoxides and epoxy alcohols have been opened to the corresponding halohydrins by lithium halides with Amberlyst in CH3CN at room temperature: the reaction proceeds in quantitative yields with high degree of regioselectivity.
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