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New Entry to γ-Butyrolactams by Free Radical Cyclization of <i>N</i>-Allyl-α-chloro-α-(methylthio)acetamides. Formal Total Synthesis of (±)-Pseudoheliotridane
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Citations
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References
1987
Year
EngineeringFree Radical CyclizationNatural SciencesDiversity-oriented SynthesisAbstract Tributyltin Hydride-azobisisobutyronitrileRadical CyclizationOrganic ChemistryFormal Total SynthesisAfforded γ-ButyrolactamsChemistryNew EntryHeterocycle ChemistryPharmacologySynthetic ChemistryBiomolecular EngineeringNatural Product Synthesis
Abstract Tributyltin hydride-azobisisobutyronitrile induced radical cyclization of N-allyl-α-chloro-α-(methylthio)acetamides afforded γ-butyrolactams. This method was applied to the formal total synthesis of (±)-pseudoheliotridane.
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