N-Alkylation of amines through hydrogen borrowing over a heterogeneous Cu catalyst (Articolo in rivista)

Type
Label
  • N-Alkylation of amines through hydrogen borrowing over a heterogeneous Cu catalyst (Articolo in rivista) (literal)
Anno
  • 2014-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1039/c3ra44364g (literal)
Alternative label
  • Santoro F.; Psaro R.; Ravasio N.; Zaccheria F. (2014)
    N-Alkylation of amines through hydrogen borrowing over a heterogeneous Cu catalyst
    in RSC advances
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Santoro F.; Psaro R.; Ravasio N.; Zaccheria F. (literal)
Pagina inizio
  • 2596 (literal)
Pagina fine
  • 2600 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://www.scopus.com/inward/record.url?eid=2-s2.0-84890594442&partnerID=q2rCbXpz (literal)
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  • 4 (literal)
Rivista
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  • 5 (literal)
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  • 6 (literal)
Note
  • Scopu (literal)
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  • CNR ISTM, via C. Golgi 19, 20133 Milan, Italy (literal)
Titolo
  • N-Alkylation of amines through hydrogen borrowing over a heterogeneous Cu catalyst (literal)
Abstract
  • Substitution of alkylhalides for the synthesis of amines is a relevant target for synthetic chemists. Secondary amines can be obtained in a one pot-one step reaction from secondary and benzylic alcohols and aniline over a heterogeneous copper catalyst. The process does not require any additive, is intrinsically safe and produces no waste. © 2014 The Royal Society of Chemistry. (literal)
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