Publication | Closed Access
Synthesis of 2-aminofurans and 2-unsubstituted furans via carbenoid-mediated [3 + 2] cycloaddition
99
Citations
27
References
2012
Year
2-Unsubstituted FuransEnantioselective SynthesisEngineeringHeterocyclicNatural SciencesDiversity-oriented SynthesisCommon IntermediatesOrganic ChemistryChemistryPharmacologySynthetic ChemistryCopper CarbenoidsBiomolecular EngineeringNatural Product Synthesis
An efficient dual synthetic manifold for 2-aminofurans and 2-unsubstituted furans has been developed. The carbenoid-mediated [3 + 2] cycloaddition of copper carbenoids with enamines provides 2-amino-2,3-dihydrofurans which serve as common intermediates for both 2-aminofurans and 2-unsubstituted furans.
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