New synthetic approach to atypical retinoids: application of a versatile annulation procedure (Articolo in rivista)

Type
Label
  • New synthetic approach to atypical retinoids: application of a versatile annulation procedure (Articolo in rivista) (literal)
Anno
  • 2007-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/j.tet.2006.12.038 (literal)
Alternative label
  • Brenna E., Fuganti C., Fronza G., Gatti F.G., Sala F., Serra S. (2007)
    New synthetic approach to atypical retinoids: application of a versatile annulation procedure
    in Tetrahedron (Oxf., Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Brenna E., Fuganti C., Fronza G., Gatti F.G., Sala F., Serra S. (literal)
Pagina inizio
  • 2351 (literal)
Pagina fine
  • 2356 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 63 (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
  • New synthetic approach to atypical retinoids: application of a versatile annulation procedure (literal)
Abstract
  • A new approach to an atypical retinoid is presented. The C-15 skeleton was built up by exploiting a step-by-step sequence: the C-9 fragment of an intermediate was homologated by reaction with a C-4 phosphorane, and then submitted to a benzannulation reaction. The last two carbon atoms were inserted by a Wittig reaction with the C-2 phosphorane of ethyl bromoacetate. Manipulation of functional groups was then performed. (literal)
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