Abstract
A cobalt-N-heterocyclic carbene catalyst allows ortho-alkylation of aromatic imines with unactivated primary and secondary alkyl chlorides and bromides under room-temperature conditions. The scope of the reaction encompasses or complements that of cobalt-catalyzed ortho-alkylation reactions with olefins as alkylating agents that we developed previously. Stereochemical outcomes of secondary alkylation reactions suggest that the reaction involves single-electron transfer from a cobalt species to the alkyl halide to generate the corresponding alkyl radical. A cycloalkylated product obtained by this method can be transformed into unique spirocycles through manipulation of the directing group and the cycloalkyl groups. © 2014 IUPAC.
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Yoshikai, N., & Gao, K. (2014). Cobalt-catalyzed directed alkylation of arenes with primary and secondary alkyl halides. In Pure and Applied Chemistry (Vol. 86, pp. 419–424). IUPAC Secretariat. https://doi.org/10.1515/pac-2014-5005
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