Palladium-catalyzed cyclization of N-n-butyl, N-(o-iodobenzyl)-3-butenamides: six- versus seven- and eight-membered ring formation (Articolo in rivista)

Type
Label
  • Palladium-catalyzed cyclization of N-n-butyl, N-(o-iodobenzyl)-3-butenamides: six- versus seven- and eight-membered ring formation (Articolo in rivista) (literal)
Anno
  • 2002-01-01T00:00:00+01:00 (literal)
Alternative label
  • Ferraccioli R. 1, Carenzi D. 2, Catellani M. 3. (2002)
    Palladium-catalyzed cyclization of N-n-butyl, N-(o-iodobenzyl)-3-butenamides: six- versus seven- and eight-membered ring formation
    in Synlett (Stuttg.)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Ferraccioli R. 1, Carenzi D. 2, Catellani M. 3. (literal)
Pagina inizio
  • 1860 (literal)
Pagina fine
  • 1864 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 11 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#descrizioneSinteticaDelProdotto
  • Sintesi non convenzionale di derivati 2-benzazepinici, 2-benzazocinici, isochinolinici, basata sull'impiego catalitico di complessi del palladio in un mezzo organico, in presenza ed in assenza di acqua (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • 1: ISTM-CNR 2: Università degli Studi di Milano 3: Università degli Studi di Parma (literal)
Titolo
  • Palladium-catalyzed cyclization of N-n-butyl, N-(o-iodobenzyl)-3-butenamides: six- versus seven- and eight-membered ring formation (literal)
Abstract
  • Potentially bio-active 2-benzazepine, 2-benzazocine, isoquinoline derivatives were selectively synthesized from N-alkyl, N-(o-iodobenzyl)-3-butenamides and a catalytic amount of palladium complexes. The regiochemistry of the annulation leading to seven/eight- or six-membered ring formation can be completely determined varying medium polarity by the addition of water (literal)
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