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Development of a Nickel-Catalyzed N–N Coupling for the Synthesis of Hydrazides

[Image: see text] A nickel-catalyzed N–N cross-coupling for the synthesis of hydrazides is reported. O-Benzoylated hydroxamates were efficiently coupled with a broad range of aryl and aliphatic amines via nickel catalysis to form hydrazides in an up to 81% yield. Experimental evidence implicates the...

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Detalles Bibliográficos
Autores principales: Barbor, Jay P., Nair, Vaishnavi N., Sharp, Kimberly R., Lohrey, Trevor D., Dibrell, Sara E., Shah, Tejas K., Walsh, Martin J., Reisman, Sarah E., Stoltz, Brian M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10360072/
https://www.ncbi.nlm.nih.gov/pubmed/37413695
http://dx.doi.org/10.1021/jacs.3c04834
Descripción
Sumario:[Image: see text] A nickel-catalyzed N–N cross-coupling for the synthesis of hydrazides is reported. O-Benzoylated hydroxamates were efficiently coupled with a broad range of aryl and aliphatic amines via nickel catalysis to form hydrazides in an up to 81% yield. Experimental evidence implicates the intermediacy of electrophilic Ni-stabilized acyl nitrenoids and the formation of a Ni(I) catalyst via silane-mediated reduction. This report constitutes the first example of an intermolecular N–N coupling compatible with secondary aliphatic amines.