Hydrogenation of ortho-nitrochalcones over Pd/C as simple access to 2-substituted 1,2,3,4-tetrahydroquinolines (Articolo in rivista)

Type
Label
  • Hydrogenation of ortho-nitrochalcones over Pd/C as simple access to 2-substituted 1,2,3,4-tetrahydroquinolines (Articolo in rivista) (literal)
Anno
  • 2010-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/j.tet.2010.05.090 (literal)
Alternative label
  • Angela Patti; Sonia Pedotti (2010)
    Hydrogenation of ortho-nitrochalcones over Pd/C as simple access to 2-substituted 1,2,3,4-tetrahydroquinolines
    in Tetrahedron (Oxf., Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Angela Patti; Sonia Pedotti (literal)
Pagina inizio
  • 5607 (literal)
Pagina fine
  • 5611 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://www.sciencedirect.com/science/article/pii/S0040402010008446 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 66 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
  • 5 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 30 (literal)
Note
  • ISI Web of Science (WOS) (literal)
  • Scopu (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • Istituto di Chimica Biomolecolare del CNR, via Paolo Gaifami 18, I-95126 Catania, Italy (literal)
Titolo
  • Hydrogenation of ortho-nitrochalcones over Pd/C as simple access to 2-substituted 1,2,3,4-tetrahydroquinolines (literal)
Abstract
  • The preparation of some 2-substituted-1,2,3,4-tetrahydroquinoline has been achieved by the one-pot reductive intramolecular cyclization of ortho-nitrochalcones with gaseous hydrogen in the presence of a Pd/C catalyst and the best selectivity was observed using CH2Cl2 as solvent. The method is operationally simple and versatile since ortho-nitrocalchones are easily accessible by Claisen-Schmidt condensation of 2-nitrobenzaldehydes and enolizable ketones. Selected examples on structurally different substrates have been considered and a novel tetrahydroquinoline and a benzo[h]tetrahydroquinoline were prepared and characterised. (literal)
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