Stereoselective synthesis of a functionalized 2-oxo-1-azabicyclo[5.3.0]alkane as a potential scaffold for targeted chemotherapy strategieseted chemoterapy strategies (Articolo in rivista)

Type
Label
  • Stereoselective synthesis of a functionalized 2-oxo-1-azabicyclo[5.3.0]alkane as a potential scaffold for targeted chemotherapy strategieseted chemoterapy strategies (Articolo in rivista) (literal)
Anno
  • 2003-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1055/s-2003-42400 (literal)
Alternative label
  • Bracci A.; Manzoni L.; Scolastico C. (2003)
    Stereoselective synthesis of a functionalized 2-oxo-1-azabicyclo[5.3.0]alkane as a potential scaffold for targeted chemotherapy strategieseted chemoterapy strategies
    in Synthesis (Stuttg.)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Bracci A.; Manzoni L.; Scolastico C. (literal)
Pagina inizio
  • 2363 (literal)
Pagina fine
  • 2367 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Bracci A.; Scolastico C.; Università degli Studi di Milano, Dipartimento di Chimica Organica e Industriale, Via Venezian 21, I-20133 Milano, Italy and CISI Manzobi L.; CNR - Istituto di Scienze e Tecnologiwe Molecolari, Via Golgi 19, I-20133 Milano, Italy (literal)
Titolo
  • Stereoselective synthesis of a functionalized 2-oxo-1-azabicyclo[5.3.0]alkane as a potential scaffold for targeted chemotherapy strategieseted chemoterapy strategies (literal)
Abstract
  • A stereoselective synthesis of functionalized 2-oxo-1-azabicyclo[5.3.0]alkane is presented. Key events of the synthetic sequence were the stereoselective propenylation of an N-acyliminium ion and a ring-closing metathesis reaction forming a 7-membered lactam. (literal)
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