Expanding the toolbox of Baeyer-Villiger and flavin monooxygenase biocatalysts for the enantiodivergent green synthesis of sulfoxides

Two new monooxygenase biocatalysts, the Baeyer-Villiger monooxygenase BVMO145 and the flavin monooxygenase FMO401 from Almac library, have been found to catalyse the enantiodivergent oxidation of sulfides bearing N-heterocyclic substituents into sulfoxides under mild and green conditions. The biocat...

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Veröffentlicht in:Green chemistry : an international journal and green chemistry resource : GC 2024-07, Vol.26 (15), p.8685-8693
Hauptverfasser: Wu, Jingyue, Anselmi, Silvia, Carvalho, Alexandra T. P, Caswell, Jill, Quinn, Derek J, Moody, Thomas S, Castagnolo, Daniele
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Sprache:eng
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Zusammenfassung:Two new monooxygenase biocatalysts, the Baeyer-Villiger monooxygenase BVMO145 and the flavin monooxygenase FMO401 from Almac library, have been found to catalyse the enantiodivergent oxidation of sulfides bearing N-heterocyclic substituents into sulfoxides under mild and green conditions. The biocatalyst BVMO145 provides ( S )-sulfoxides while the flavin monooxygenase FMO401 affords ( R )-sulfoxides with good conversions and high ee. Two new monooxygenase biocatalysts, BVMO145 and FMO401 from Almac library, catalyse the enantiodivergent oxidation of sulfides bearing N-heterocyclic substituents into sulfoxides under mild and green conditions.
ISSN:1463-9262
1463-9270
1463-9262
DOI:10.1039/d4gc02657h