Abstract
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.
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CITATION STYLE
Barbor, J. P., Nair, V. N., Sharp, K. R., Lohrey, T. D., Dibrell, S. E., Shah, T. K., … Stoltz, B. M. (2023). Development of a Nickel-Catalyzed N-N Coupling for the Synthesis of Hydrazides. Journal of the American Chemical Society, 145(28), 15071–15077. https://doi.org/10.1021/jacs.3c04834
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