Primary CH bond activation! A Rh complex of bis-pocket porphyrin I catalyzes carbenoid insertion into the CH bonds of n-alkanes with a primary/secondary selectivity (per CH bond) of up to 11.4:1 (see picture). Enantioselective secondary CH bond functionalization catalyzed by a Rh complex of Halterman's chiral porphyrin features up to 93 % ee. These reactions exhibit up to 6477 turnovers after the catalyst was recycled five times.
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Tong et al. (2008) studied this question.
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