A new entry to the substituted Pyrrolo[3,2-c]quinoline derivatives of biological interest by intramolecular heteroannulation of internal imines (Articolo in rivista)

Type
Label
  • A new entry to the substituted Pyrrolo[3,2-c]quinoline derivatives of biological interest by intramolecular heteroannulation of internal imines (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.tet.2004.05.047 (literal)
Alternative label
  • Testa, Maria Luisa (1); Lamartina, Liliana (2); Mingoia, Francesco* (1) (2004)
    A new entry to the substituted Pyrrolo[3,2-c]quinoline derivatives of biological interest by intramolecular heteroannulation of internal imines
    in Tetrahedron (Oxf., Print); Pergamon-Elsevier Science Ltd., Oxford (Regno Unito)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Testa, Maria Luisa (1); Lamartina, Liliana (2); Mingoia, Francesco* (1) (literal)
Pagina inizio
  • 5873 (literal)
Pagina fine
  • 5880 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://scienceserver.cilea.it/cgi-bin/sciserv.pl?collection=journals&journal=00404020&issue=v60i0028 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 60 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
  • 8 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 28 (literal)
Note
  • ISI Web of Science (WOS) (literal)
  • Google Scholar (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • (1) Ist. Stud. Materiali Nanostrutturati - I.S.M.N.-C.N.R, Palermo; (2) Dipto. Chim. Tecnologie F. - Universit√† di Palermo; (literal)
Titolo
  • A new entry to the substituted Pyrrolo[3,2-c]quinoline derivatives of biological interest by intramolecular heteroannulation of internal imines (literal)
Abstract
  • New 1,3,4-substituted pyrrolo[3,2-c]quinoline derivatives were synthesised in good yields by oxidative heteroannulation of internal imines starting from easily prepared substituted 5-(2-aminophenyl)pyrroles and commercially available aryl and heteroaryl aldehydes. The reaction occurs as a one-pot process involving an intramolecular (literal)
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