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Synthesis of Benzoxazines by Heterogeneous Multicomponent Biochemo Multienzymes Cascade Reaction.
Tomaino, Elisabetta; Capecchi, Eliana; Ubertini, Valentina; Piccinino, Davide; Bizzarri, Bruno M; Saladino, Raffaele.
Afiliación
  • Tomaino E; Department of Biological and Ecological Sciences, University of Tuscia, Via San Camillo De Lellis s.n.c., Viterbo 01100, Italy.
  • Capecchi E; Department of Biological and Ecological Sciences, University of Tuscia, Via San Camillo De Lellis s.n.c., Viterbo 01100, Italy.
  • Ubertini V; Department of Biological and Ecological Sciences, University of Tuscia, Via San Camillo De Lellis s.n.c., Viterbo 01100, Italy.
  • Piccinino D; Department of Biological and Ecological Sciences, University of Tuscia, Via San Camillo De Lellis s.n.c., Viterbo 01100, Italy.
  • Bizzarri BM; Department of Biological and Ecological Sciences, University of Tuscia, Via San Camillo De Lellis s.n.c., Viterbo 01100, Italy.
  • Saladino R; Department of Biological and Ecological Sciences, University of Tuscia, Via San Camillo De Lellis s.n.c., Viterbo 01100, Italy.
J Org Chem ; 89(4): 2343-2350, 2024 Feb 16.
Article en En | MEDLINE | ID: mdl-38284895
ABSTRACT
This work describes the possibility to combine multicomponent chemistry and multienzymes cascade transformations in a unique reactive framework to yield highly functionalized 1,4-benzoxazines under favorable heterogeneous conditions. The synthetic scheme involved the generation in situ of electrophilic reactive quinone intermediates of tyrosol esters catalyzed by lipase M and tyrosinase followed by nucleophilic 1,6-Michael addition of selected α-amino acid methyl esters, and successive intramolecular lactonization and aromatization processes. The immobilization of the multienzymes cascade on electroactive lignin nanoparticles improved the sustainability and recyclability of the overall system.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Org Chem / J. org. chem / Journal of organic chemistry Año: 2024 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: J Org Chem / J. org. chem / Journal of organic chemistry Año: 2024 Tipo del documento: Article País de afiliación: Italia
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