Enzymatic Baeyer-Villiger oxidation of bicyclic diketones (Articolo in rivista)

Type
Label
  • Enzymatic Baeyer-Villiger oxidation of bicyclic diketones (Articolo in rivista) (literal)
Anno
  • 2005-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1002/adsc.200505027 (literal)
Alternative label
  • Ottolina G., de Gonzalo G., Carrea G., Danieli B. (2005)
    Enzymatic Baeyer-Villiger oxidation of bicyclic diketones
    in Advanced synthesis & catalysis (Print); Wiley-VCH Verlag Gmbh, Weinheim (Germania)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Ottolina G., de Gonzalo G., Carrea G., Danieli B. (literal)
Pagina inizio
  • 1035 (literal)
Pagina fine
  • 1040 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://onlinelibrary.wiley.com/doi/10.1002/adsc.200505027/abstract (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 347 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 7-8 (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Istituto di Chimica del Riconoscimento Molecolare, CNR ,Via Mario Bianco 9, 20131 Milano, Italy Dipartimento di Chimica Organica e Industriale, Università degli Studi di Milano, Via Venezian 21, 20133 Milano, Italy (literal)
Titolo
  • Enzymatic Baeyer-Villiger oxidation of bicyclic diketones (literal)
Abstract
  • Cyclohexanone monooxygenase from Acinetobacter calcoaceticus was employed for the Baeyer-Villiger oxidation of racemic bicyclic diketones such as the Wieland-Miescher and the Hajos-Parrish diketones and of some of their derivatives. The corresponding lactones were produced in a highly regio- and enantioselective manner. The reactions were carried out using a crude enzyme preparation in aqueous buffer, at room temperature, and the recycling of the expensive coenzyme NADPH was conducted with a second ancillary enzymatic system. The enzymatic process was simple and easy to handle, thus providing a very practical tool to access enantiopure lactones. (literal)
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