Organic Letters · 2010 · 66 citations · 43 references
Natural SciencesChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySynthetic Medicinal ChemistryCross-coupling ReactionsDiversity-oriented SynthesisHeterocycle SynthesisOrganic SynthesisReaction MechanismsDouble BondsIntermediate InputsLactam MacrocyclesLactam SynthesisMulticomponent Reaction ChemistryQuinoline ChemistryQuinoline Synthesis
Unsaturated lactams with endo- or exocyclic C-C double bonds constitute a set of reactive inputs that serve as the electron-rich olefin component in Povarov reactions. These substrates afford the multicomponent adducts in convenient yields and offer a wide range of structural diversity. Postcondensation transformations allow direct access to a variety of lactam-fused and amide-substituted quinoline derivatives.
43
Scandium Triflate in Organic Synthesis
Shu̅ Kobayashi · European Journal of Organic Chemistry · 1999 · 435 citations