Angewandte Chemie International Edition · 2021 · 69 citations · 116 references
Natural SciencesChemistryMedicinal ChemistryCatalysisOrganic ChemistrySynthetic Medicinal ChemistryCatalytic MechanismsCross-coupling ReactionsOrganic SynthesisAlkylation ReactionsAsymmetric CatalysisChiral Product SynthesisEnantioselective Synthesis
A variety of inert tertiary amides have been successfully transformed into synthetically important chiral propargylamines in high yields with good to excellent enantioselectivities via a relayed sequence of Ir catalyzed partial reduction and Cu/GARPHOS catalyzed asymmetric alkynylation with terminal alkynes. The reaction was readily extended to some drug molecules and the transformations of representative products have been demonstrated, thus attesting the practical utilities and the robust nature of the protocol.
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Conversion of amides to esters by the nickel-catalysed activation of amide C–N bonds
Liana Hie, Noah F. Fine Nathel, Tejas K. Shah et al. · Nature · 2015 · 559 citations · Full text