European Journal of Organic Chemistry · 2018 · 131 citations · 121 references
PharmacyBiochemistryMedicinal ChemistryBiocatalysisDrug DiscoverySynthetic Medicinal ChemistryCatalytic MechanismsCross-coupling ReactionsEnzyme-substrate RecognitionPeptide Bond ChemistryPeptide ChemistryScaffold DiversificationAmide Bond FormationMechanistic Studies Of Cross-couplingPeptide Coupling ReagentsPrivileged Ring ScaffoldsPrivileged Scaffold Libraries
In this Microreview, we describe the recent exciting developments in the burgeoning area of amide N–C cross‐coupling enabled by amide bond twist of N ‐acyl‐glutarimides. Since the initial reports in 2015, these amides have been demonstrated to be by far the most reactive amide derivatives in the biologically‐relevant manifold of N–C activation/cross‐coupling, thus stimulating the development of more than 10 previously unknown catalytic modes of reactivity of the amide bond. The capacity of N ‐acyl‐glutarimides as privileged scaffolds to expedite acyl and decarbonylative cross‐couplings by amide N–C cleavage is discussed.
121
Goodman and Gilman's the Pharmacological Basis of Therapeutics
William H. Stigelman, D Pharm · Military Medicine · 1986 · 6.8K citations
N-methoxy-n-methylamides as effective acylating agents
Steven Nahm, Steven M. Weinreb · Tetrahedron Letters · 1981 · 1.8K citations