From chiral and prochiral N-allylpyrroles to stereodefined pyrrole fused architectures: a particular application of the rhodium catalyzed hydroformylation (Articolo in rivista)

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Label
  • From chiral and prochiral N-allylpyrroles to stereodefined pyrrole fused architectures: a particular application of the rhodium catalyzed hydroformylation (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.jorganchem.2006.11.020 (literal)
Alternative label
  • Lazzaroni R.; Settambolo R.; Rocchiccioli S.; Guazzelli G. (2007)
    From chiral and prochiral N-allylpyrroles to stereodefined pyrrole fused architectures: a particular application of the rhodium catalyzed hydroformylation
    in Journal of organometallic chemistry (Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Lazzaroni R.; Settambolo R.; Rocchiccioli S.; Guazzelli G. (literal)
Pagina inizio
  • 1812 (literal)
Pagina fine
  • 1816 (literal)
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  • Prodotto digitalizzato (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 692 (literal)
Rivista
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • L. R.: DCCI Università di Pisa, Pisa, S. R.: ICCOM-CNR Sezione di Pisa, Pisa; R. S.: DCCI Università di Pisa, Pisa; G. G.: DCCI Università di Pisa, Pisa (literal)
Titolo
  • From chiral and prochiral N-allylpyrroles to stereodefined pyrrole fused architectures: a particular application of the rhodium catalyzed hydroformylation (literal)
Abstract
  • We review our recent results on the rhodium-catalyzed hydroformylation of chiral and prochiral N-allylpyrroles as a synthetic route to stereodefined 5,6-dihydro- and 5,6,7,8-tetrahydroindolizines. The indolizine nucleus at different degrees of unsaturation is a building block of natural and synthetic target compounds; thus new approaches, especially if stereoselective and/or stereospecific, are highly desirable. The construction of the indolizine architectures reported here occurs by formation of a C8-C9 bond through intramolecular cyclization of the 4-pyrrolylbutanal intermediate. © 2006 Elsevier B.V. All rights reserved. (literal)
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