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Expanding the toolbox of Baeyer-Villiger and flavin monooxygenase biocatalysts for the enantiodivergent green synthesis of sulfoxides.
Wu, Jingyue; Anselmi, Silvia; Carvalho, Alexandra T P; Caswell, Jill; Quinn, Derek J; Moody, Thomas S; Castagnolo, Daniele.
Afiliação
  • Wu J; Department of Chemistry, University College London 20 Gordon Street WC1H 0AJ London UK d.castagnolo@ucl.ac.uk.
  • Anselmi S; Department of Chemistry, University College London 20 Gordon Street WC1H 0AJ London UK d.castagnolo@ucl.ac.uk.
  • Carvalho ATP; Department of Biocatalysis & Isotope Chemistry Almac 20 Seagoe Industrial Estate Craigavon BT63 5QD UK tom.moody@almacgroup.com.
  • Caswell J; Department of Biocatalysis & Isotope Chemistry Almac 20 Seagoe Industrial Estate Craigavon BT63 5QD UK tom.moody@almacgroup.com.
  • Quinn DJ; Department of Biocatalysis & Isotope Chemistry Almac 20 Seagoe Industrial Estate Craigavon BT63 5QD UK tom.moody@almacgroup.com.
  • Moody TS; Department of Biocatalysis & Isotope Chemistry Almac 20 Seagoe Industrial Estate Craigavon BT63 5QD UK tom.moody@almacgroup.com.
  • Castagnolo D; Arran Chemical Company Limited, Unit 1 Monksland Industrial Estate Athlone Co. Roscommon Ireland.
Green Chem ; 26(15): 8685-8693, 2024 Jul 29.
Article em En | MEDLINE | ID: mdl-39081496
ABSTRACT
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.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Green Chem Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Green Chem Ano de publicação: 2024 Tipo de documento: Article