Enzyme-catalysed apporach to the preparatoin of triazole antifungals: Synthesis of (-)-genaconazole (Articolo in rivista)

Type
Label
  • Enzyme-catalysed apporach to the preparatoin of triazole antifungals: Synthesis of (-)-genaconazole (Articolo in rivista) (literal)
Anno
  • 2009-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/j.tetasy.2009.09.024 (literal)
Alternative label
  • Acetti D., Brenna E., Fuganti C., Gatti F.G., Serra S. (2009)
    Enzyme-catalysed apporach to the preparatoin of triazole antifungals: Synthesis of (-)-genaconazole
    in Tetrahedron: asymmetry (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Acetti D., Brenna E., Fuganti C., Gatti F.G., Serra S. (literal)
Pagina inizio
  • 2413 (literal)
Pagina fine
  • 2420 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 20 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • CNR-ICRM Politecnico di Milano (literal)
Titolo
  • Enzyme-catalysed apporach to the preparatoin of triazole antifungals: Synthesis of (-)-genaconazole (literal)
Abstract
  • The work describes a new enzyme-mediated approach to optically active epoxide (2R,3S)-6, which is an important key intermediate in the preparation of single enantiomers of chiral azole antifungals. The conversion of (2R,3S)-6 into (-)-genaconazole is reported as an example of its synthetic relevance. (literal)
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