Publication | Closed Access
Enantioselective [4 + 2]-Annulation of Oxadienes and Allenones Catalyzed by an Amino Acid Derived Phosphine: Synthesis of Functionalized Dihydropyrans
58
Citations
78
References
2016
Year
Cyano-activated OxadienesChemical EngineeringNovel OrganocatalystsEngineeringWide RangeL-valine-derived PhosphineOrganic ChemistryOrganometallic CatalysisCatalysisChemistryHeterocycle ChemistryFunctionalized DihydropyransAsymmetric CatalysisSynthetic ChemistryEnantioselective SynthesisAllenones Catalyzed
An enantioselective [4 + 2]-annulation process between cyano-activated oxadienes and allenones is developed. An l-valine-derived phosphine was efficient in catalyzing the reaction, and a wide range of highly functionalized dihydropyrans were prepared in high yields and with excellent enantioselectivities.
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