Convenient access to both enantiomers of new azido- and aminoinositols via a chemoenzymatic route (Articolo in rivista)

Type
Label
  • Convenient access to both enantiomers of new azido- and aminoinositols via a chemoenzymatic route (Articolo in rivista) (literal)
Anno
  • 1998-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/S0957-4166(98)00271-7 (literal)
Alternative label
  • Sanfilippo, Claudia, Patti, Angela, Piattelli, Mario, Nicolosi, Giovanni (1998)
    Convenient access to both enantiomers of new azido- and aminoinositols via a chemoenzymatic route
    in Tetrahedron: asymmetry (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Sanfilippo, Claudia, Patti, Angela, Piattelli, Mario, Nicolosi, Giovanni (literal)
Pagina inizio
  • 2809 (literal)
Pagina fine
  • 2817 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 9 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 16 (literal)
Note
  • Scopus (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Istituto CNR Studio Sostanze Naturali di Interesse Alimentare e Chimico-Farmaceutico (literal)
Titolo
  • Convenient access to both enantiomers of new azido- and aminoinositols via a chemoenzymatic route (literal)
Abstract
  • 1,2-diacetylconduritol E, (±)-1, through complementary use of Mucor miehei (Lipozyme® IM) and Candida cylindracea lipases, affords (1S)-1,2-diacetylconduritol E, (+)-1, (1R)-1,2-diacetylconduritol E, (-)-1, (1S)-1,2,4-triacetylconduritol E, (+)-2, (1R)-1,2,4-triacetylconduritol E, (-)-2, with high enantiomeric excesses and chemical yields. Following two different methods, diester (+)-1 has been transformed into azidoinositol (-)-4 to give 1L-4-amino-4-deoxy-chiro-inositol, whereas triester (-)-2 furnished the azidoinositol (+)-13, easily converted into 1L-4-amino-4-deoxy-myo-inositol. (literal)
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