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Aminocatalytic Strategy for the Synthesis of Optically Active Benzothiophene Derivatives
40
Citations
32
References
2016
Year
EngineeringSynthetic PhotochemistryOrganic ChemistryChemistryHeterocycle ChemistryAromatic Benzothiophene MoietyAminocatalytic StrategyBenzothiophene DerivativesStereoselective SynthesisDerivativesPhotochemistryAdjacent Stereogenic CentersDiversity-oriented SynthesisCatalysisSynthesis MethodEnantioselective SynthesisBiomolecular EngineeringHeterocyclicNatural SciencesSynthetic Chemistry
Abstract A novel approach for the stereoselective synthesis of benzothiophene derivatives with a fused dihydropyran moiety is demonstrated. The reaction of 2‐alkylidenebenzothiophene‐3(2 H )‐ones with dienamines derived from α,β‐unsaturated aldehydes and chiral secondary amines proceeds according to the inverse‐electron‐demand hetero‐Diels–Alder pathway. The formation of the aromatic benzothiophene moiety is a driving force for the developed reaction cascade. Target products bearing three adjacent stereogenic centers are obtained in excellent yields and in a highly stereoselective manner. magnified image
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