Publication | Closed Access
Vilsmeier-Type Reaction of Dimethylaminoalkenoyl Cyclopropanes: One-Pot Access to 2,3-Dihydrofuro [3,2-<i>c</i>]pyridin-4(5<i>H</i>)-ones
44
Citations
54
References
2011
Year
Ring-enlargement SequencesEngineeringHeterocyclicOrganic ChemistryIntramolecular CyclizationChemistryDomino ReactionHeterocycle ChemistryPharmacologyStereoselective SynthesisBiomolecular EngineeringOne-pot Access
A domino reaction of readily available 1-carbamoyl-1-dimethylaminoalkenoylcyclopropanes in the presence of triflic anhydride (Tf(2)O) in N,N-dimethylformamide (DMF) is described, which provides a facile one-pot access to 2,3-dihydrofuro[3,2-c]pyridin-4(5H)-ones via tandem formylation (Vilsmeier-type reaction), intramolecular cyclization, and ring-enlargement sequences.
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