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Demonstrates high enantioselectivity in oxidation reactions, suggesting innovative catalytic applications.
, CoPC-BSA catalyzed epoxidations of styrene and cyclooctene with yields of 87-99%, achieving >99% enantioselectivity for R-styrene oxide. CoPC-BSA also enabled selective C-H oxidation of propanoic acid and methyl phenylacetate under mild conditions. For propanoic acid, L-lactic acid was the sole product of oxidation of propanoic acid, while methyl phenylacetate showed temperature-dependent enantioselectivity. When immobilized on silica beads, R-methyl mandelate with an enantioselectivity >92% at 80 °C was produced at a conversion of ∼99%. These results demonstrate the potential of molecular hybrids for enantioselective oxidations and highlight the critical role of protein flexibility and dynamics in tuning catalytic outcomes.
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Liaqat et al. (2026) studied this question.
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