Publication | Closed Access
Direct Access to Heterocyclic Scaffolds by New Multicomponent Ugi−Smiles Couplings
73
Citations
5
References
2006
Year
Cross-coupling ReactionSupramolecular AssemblyEngineeringHeterocyclicNatural SciencesUgi ReactionDiversity-oriented SynthesisOrganic ChemistrySmiles RearrangementNew Heterocyclic ScaffoldsChemistryCoordination PolymerHeterocycle ChemistryDirect AccessSynthetic ChemistryBiomolecular Engineering
New heterocyclic scaffolds can be easily prepared by the coupling of heteroaromatic phenols (pyridines, pyrimidines) with carbonyl compounds, amines, and isocyanides. This transformation related to the Ugi reaction probably involves a Smiles rearrangement. The scope of this methodology is further extended by the successful use of heterocyclic thiols to form highly functionalized thioamides.
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