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Coupling-Isomerization-Stetter and Coupling-Isomerization-Stetter-Paal-Knorr Sequences - A Multicomponent Approach to Furans and Pyrroles
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2004
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Combinatorial ChemistryCross-coupling ReactionEngineeringHeterocyclicChemical TransformationLinear Chain CompoundMulticomponent ApproachOrganic Chemistry2,3,5-Trisubstituted Furans 6Synthetic ChemistryChemistryHeterocycle ChemistryPrimary Amine 7Chemical KineticsNovel FuransBiomolecular EngineeringCoupling-isomerization-stetter-paal-knorr Sequences
2,3,5-Trisubstituted furans 6 and 1,2,3,5-tetrasubstituted pyrroles 8 can be synthesized in good yields in a one-pot three-step three- or four-component process by a coupling-isomerization-Stetter-Paal-Knorr sequence of an electron-poor (hetero)aryl halide 1, a terminal propargyl alcohol 2, an aldehyde 3, and, in the case of pyrroles, a primary amine 7. All novel furans and pyrroles exhibit a strong blue fluorescence with considerable Stokes shifts.