Ruthenium(ii)-catalyzed acyloxylation of the ortho-C–H bond in 2-aroyl-imidazoles with carboxylic acids‡

Literature Information

Publication Date 2020-08-31
DOI 10.1039/D0QO00920B
Impact Factor 5.281
Authors

Chen-an Wang, Naoto Chatani


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Abstract

The reaction of 2-aroyl-imidazoles with carboxylic acids using [RuCl2(p-cymene)]2 as the catalyst and Ag2CO3 as the oxidant results in ortho-C–H acyloxylation to afford acyloxylation products, in which the imidazole group functions as a directing group. A wide range of functional groups are tolerated in the reaction. The directing group can be easily converted to the corresponding esters under mild conditions.

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