Stereoselective cyclopropanation of chiral 5-substituted dihydro-2H-piperazines (Articolo in rivista)

Type
Label
  • Stereoselective cyclopropanation of chiral 5-substituted dihydro-2H-piperazines (Articolo in rivista) (literal)
Anno
  • 2013-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/j.tetasy.2012.11.015 (literal)
Alternative label
  • Reginato, Gianna; Catalani, Maria Pia; Mordini, Alessandro Mordini; Pezzati, Bernardo Pezzati; Bernardelli, Andrea; Davalli, Silvia; Pace, Nicola (2013)
    Stereoselective cyclopropanation of chiral 5-substituted dihydro-2H-piperazines
    in Tetrahedron: asymmetry (Online)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Reginato, Gianna; Catalani, Maria Pia; Mordini, Alessandro Mordini; Pezzati, Bernardo Pezzati; Bernardelli, Andrea; Davalli, Silvia; Pace, Nicola (literal)
Pagina inizio
  • 75 (literal)
Pagina fine
  • 79 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 24 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
  • 4 (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Aptuit, Medicine Research Center (literal)
Titolo
  • Stereoselective cyclopropanation of chiral 5-substituted dihydro-2H-piperazines (literal)
Abstract
  • The Simmon-Smith cyclopropanation of enantiomerically enriched dehydropiperazines is reported. The reaction is highly stereoselective and allowed us to prepare new, enantiomerically enriched 3-substituted 2,5-diazabicyclo[4.1.0]heptane cores with high diastereomeric purity and a relative anti-configuration, which was assigned by NMR analysis (literal)
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