Stereoselective chemo-enzymatic approaches to the synthesis of C2 1,3-dithiane-1,3-dioxide (Articolo in rivista)

Type
Label
  • Stereoselective chemo-enzymatic approaches to the synthesis of C2 1,3-dithiane-1,3-dioxide (Articolo in rivista) (literal)
Anno
  • 2009-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1080/10426500902856446 (literal)
Alternative label
  • Gaggero N., Colonna S., Albanese D., Ottolina G., Del Monte F. (2009)
    Stereoselective chemo-enzymatic approaches to the synthesis of C2 1,3-dithiane-1,3-dioxide
    in Phosphorus, sulfur, and silicon and the related elements; Gordon and Breach, New York (Stati Uniti d'America)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Gaggero N., Colonna S., Albanese D., Ottolina G., Del Monte F. (literal)
Pagina inizio
  • 1332 (literal)
Pagina fine
  • 1339 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://www.tandfonline.com/doi/abs/10.1080/10426500902856446 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 184 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 5 (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Ist Chim Organ A Marchesini, I-20133 Milan, Italy Univ Milan, Dipartimento Chim Organ & Ind, Milan, Italy CNR, Ist Chim Riconoscimento Mol, I-20133 Milan, Italy (literal)
Titolo
  • Stereoselective chemo-enzymatic approaches to the synthesis of C2 1,3-dithiane-1,3-dioxide (literal)
Abstract
  • Two enzyme-mediated methods are presented for the preparation of enantiomerically enriched C 2 1,3-dithiane-1,3-dioxide. The first takes advantage of a trans stereoselective oxidation by NaIO 4 of enantiomerically pure (R) 1,3-dithiane-1-oxide obtained by cyclohexanone monooxygenase. In the second method, a kinetic resolution consisting of a domino hydrolysis-decarboxylation process of (±) 2-carbethoxy-1,3-dithiane-trans-1,3-dioxide is described. The target molecule is obtained with enantiomeric excesses up to 90%. (literal)
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