C-H and N-H Bond Annulation of Benzamides with Isonitriles Catalyzed by Cobalt(III)

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Abstract

A simple efficient, atom-economical procedure was developed for the cobalt-catalyzed C-H bond annulation of benzamides with isonitriles under mild conditions. The reaction tolerates a variety of functional group including heterocycles. Diverse 3-(alkylimino)-2-quinolin-8-yl-2,3-dihydro-1 H -isoindol-1-ones were synthesized using isonitriles as the C1 source through C-H and N-H bond annulation via C-H bond activation in a 'green' solvent. Vinylamides were also used similarly with tert -butyl isonitrile to give 3-(tert -butylimino)-1-quinolin-8-yl-1 H -pyrrol-2(5 H)-ones.

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Kalsi, D., Barsu, N., Dahiya, P., & Sundararaju, B. (2017). C-H and N-H Bond Annulation of Benzamides with Isonitriles Catalyzed by Cobalt(III). Synthesis (Germany), 49(17), 3937–3944. https://doi.org/10.1055/s-0036-1589011

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