The facile oxidation of alcohols to carboxylate salts and H is achieved using a simple and readily accessible cobalt pincer catalyst (NNNCoBr). The reaction follows an acceptorless dehydrogenation pathway and displays good functional group tolerance. The amine-amide metal-ligand cooperation in cobalt catalyst is suggested to facilitate this transformation. The mechanistic studies indicate that in-situ-formed aldehydes react with a base through a Cannizzaro-type pathway, resulting in potassium hemiacetolate, which further undergoes catalytic dehydrogenation to provide the carboxylate salts and H.
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http://dx.doi.org/10.1021/acs.orglett.0c00193 | DOI Listing |
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