Described here is a synthetic approach to access two of the most widely invoked cationic cobaltacycles in Cp*CoIII-catalyzed C−H functionalization reactions by C−H activation. The unique stabilizing capability of MeCN was used to surmount the previously proposed reversible nature of the C−H metalation step. Moreover, it is revealed the boosting effect of 1,1,1,3,3,3-hexafluoroisopropanol in the metalation step and in the reaction between N-pyrimidinylindole and diphenylacetylene under catalytic conditions.
Sanjosé-Orduna, J.; Sarria Toro, J. M.; Pérez-Temprano, M. H.
Angew. Chem. Int. Ed. 2018, 57, (35), 11369-11373
DOI:
10.1002/anie.201806847
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