Broadening the scope of Baeyer–Villiger monooxygenase activities toward α,β-unsaturated ketones: A promising route to chiral enol-lactones and ene-lactones

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Abstract

Three regiodivergent Baeyer–Villiger mono-oxygenases (enantioselectively) oxidized a series of cyclic α,β-unsaturated ketones into (chiral) either enol-lactones or ene-lactones. An easy-to-use and efficient biocatalytic process based on a host-microorganism deprived of unwanted activities (knock-out mutant) was developed to enable the exclusive synthesis of unsaturated lactones. © Partner Organisations 2014.

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Reignier, T., de Berardinis, V., Petit, J. L., Mariage, A., Hamzé, K., Duquesne, K., & Alphand, V. (2014). Broadening the scope of Baeyer–Villiger monooxygenase activities toward α,β-unsaturated ketones: A promising route to chiral enol-lactones and ene-lactones. Chemical Communications, 50(58), 7793–7796. https://doi.org/10.1039/c4cc02541e

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