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A light-driven enzymatic enantioselective radical acylation - Nature

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A light-driven enzymatic enantioselective radical acylation - Nature

Enzymes are recognized as exceptional catalysts for achieving high stereoselectivities1–3, but their ability to control the reactivity and stereoinduction of free radicals lags behind that of chemical catalysts4. Thiamine diphosphate (ThDP)-dependent enzymes5 are well-characterized systems that inspired the development of N-heterocyclic carbenes (NHCs)6–8 but have not yet been proved viable in asymmetric radical transformations.

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A light-driven enzymatic enantioselective radical acylation - Nature

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A light-driven enzymatic enantioselective radical acylation - Nature

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