Journal of the American Chemical Society · 2009 · 153 citations · 29 references
Natural SciencesChemistryMedicinal ChemistryBiocatalysisOrganic ChemistrySynthetic Medicinal ChemistryCross-coupling ReactionsHeterocycle SynthesisOrganic SynthesisOrganic Molecule SynthesisRing-forming ReactionsStereocontrolled Library SynthesisStereoselective Synthesis
A new rhodium-catalyzed carbozincation of ynamides has been developed, using diorganozinc reagents or functionalized alkylzinc halides. The reactions are highly regio- and stereoselective, allowing access to a wide range of multisubstituted enamides, which are increasingly important building blocks for organic synthesis. Utilization of the alkenylzinc intermediates in further carbon-carbon bond-forming reactions to form trisubstituted enamides is also possible.
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Ei‐ichi Negishi, Anthony O. King, Nobuhisa Okukado · The Journal of Organic Chemistry · 1977 · 890 citations
Enamides: valuable organic substrates
David R. Carbery · Organic & Biomolecular Chemistry · 2008 · 334 citations