The Journal of Organic Chemistry · 2008 · 32 citations · 42 references
Functionalized EnamineCross-coupling ReactionEngineeringNatural SciencesDiversity-oriented SynthesisTetrasubstituted PyridinesN-dimethylformamide Diethyl AcetalOrganic ChemistryUnprecedented ApproachChemistryStereoselective SynthesisEnantioselective SynthesisBiomolecular EngineeringSingle-step Reaction
We have identified a Me3SiCl-mediated three-component coupling reaction of a functionalized enamine, N,N-dimethylformamide diethyl acetal, and an internal alkyne having an electron-withdrawing group that produces 2,3,4,5-tetrasubstituted pyridine derivatives in good to excellent yields via a single-step reaction.
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De novo synthesis of substituted pyridines
Gavin D. Henry · Tetrahedron · 2004 · 700 citations
Recent developments in imino Diels–Alder reactions
Paul T. Buonora, John‐Carl Olsen, Taeboem Oh · Tetrahedron · 2001 · 403 citations