Publication | Closed Access
Synthesis of Aminocarbonyl <i>N</i>-Acylhydrazones by a Three-Component Reaction of Isocyanides, Hydrazonoyl Chlorides, and Carboxylic Acids
30
Citations
14
References
2014
Year
Diversity Oriented SynthesisCarboxylic AcidsBiochemistryNatural SciencesThree-component ReactionDiversity-oriented SynthesisHydrazonoyl Chloridesα-Aminocarbonyl N-acylhydrazonesOrganic ChemistryAvailable Hydrazonoyl ChloridesChemistryPharmacologySynthetic ChemistryEnantioselective SynthesisNitrile Imines
A novel one-pot multicomponent synthesis of α-aminocarbonyl N-acylhydrazones starting from readily available hydrazonoyl chlorides, isocyanides, and carboxylic acids is reported. The strategy exploits the ability of the carboxylic acid as a third component to suppress all competing reactions between nitrile imines and isocyanides, channeling the course of the reaction toward the formation of this novel class of compounds.
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