A stereoselective inverting sec -alkylsulfatase for the deracemization of sec -alcohols

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Abstract

A metallo-β-lactamase-type alkylsulfatase was found to catalyze the enantioselective hydrolysis of sec-alkylsulfates with strict inversion of configuration. This catalytic event, which does not have an analog in chemocatalysis, yields homochiral (S)-configurated alcohols and nonreacted sulfate esters. The latter could be converted into (S)-sec-alcohols as the sole product in up to >99% ee via a chemoenzymatic deracemization protocol on a preparative scale. © 2011 American Chemical Society.

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Schober, M., Gadler, P., Knaus, T., Kayer, H., Birner-Grünberger, R., Gülly, C., … Faber, K. (2011). A stereoselective inverting sec -alkylsulfatase for the deracemization of sec -alcohols. Organic Letters, 13(16), 4296–4299. https://doi.org/10.1021/ol201635y

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