(5R)-5-alkyl-5,6-dihydroindolizines via stereospecific domino hydroformylation/cyclodehydrationof (3R)-3-(pyrrol-1-yl)alk-1-enes (Articolo in rivista)

Type
Label
  • (5R)-5-alkyl-5,6-dihydroindolizines via stereospecific domino hydroformylation/cyclodehydrationof (3R)-3-(pyrrol-1-yl)alk-1-enes (Articolo in rivista) (literal)
Anno
  • 2004-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/j.tetasy.2004.04.045 (literal)
Alternative label
  • Settambolo R.; Guazzelli G.; Mandoli A.; Lazzaroni R. (2004)
    (5R)-5-alkyl-5,6-dihydroindolizines via stereospecific domino hydroformylation/cyclodehydrationof (3R)-3-(pyrrol-1-yl)alk-1-enes
    in Tetrahedron: asymmetry (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Settambolo R.; Guazzelli G.; Mandoli A.; Lazzaroni R. (literal)
Pagina inizio
  • 1821 (literal)
Pagina fine
  • 1823 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#altreInformazioni
  • Prodotto digitalizzato (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 15 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • G.G.: DCCI Università di Pisa, Pisa; M.A.: DCCI Università di Pisa, Pisa; L.R.: DCCI Università di Pisa, Pisa (literal)
Titolo
  • (5R)-5-alkyl-5,6-dihydroindolizines via stereospecific domino hydroformylation/cyclodehydrationof (3R)-3-(pyrrol-1-yl)alk-1-enes (literal)
Abstract
  • (5R)-5-Alkyl-5,6-dihydroindolizines 3a-c having the same high enantiomeric excess (>92%) as the corresponding starting olefins (3R)-3-(pyrrol-1-yl)alk- 1-enes 1a-c were obtained via a highly regioselective and stereospecific domino hydroformylation/cyclodehydration reaction sequence. The reasons for this configurational stability were also analyzed in the light of the general accepted rhodium catalyzed hydroformylation mechanism. © 2004 Elsevier Ltd. All rights reserved (literal)
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