http://www.cnr.it/ontology/cnr/individuo/prodotto/ID312674
Selective N-Alkylation of Arylamines with Alkyl Chloride in Ionic Liquids: Scope and Applications (Articolo in rivista)
- Type
- Label
- Selective N-Alkylation of Arylamines with Alkyl Chloride in Ionic Liquids: Scope and Applications (Articolo in rivista) (literal)
- Anno
- 2012-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1002/ejoc.201200202 (literal)
- Alternative label
Monopoli, Antonio; Cotugno, Pietro; Cortese, Marina; Calvano, Cosima Damiana; Ciminale, Francesco; Nacci, Angelo (2012)
Selective N-Alkylation of Arylamines with Alkyl Chloride in Ionic Liquids: Scope and Applications
in European journal of organic chemistry (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Monopoli, Antonio; Cotugno, Pietro; Cortese, Marina; Calvano, Cosima Damiana; Ciminale, Francesco; Nacci, Angelo (literal)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
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- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- University of Bari; Consiglio Nazionale delle Ricerche (CNR) (literal)
- Titolo
- Selective N-Alkylation of Arylamines with Alkyl Chloride in Ionic Liquids: Scope and Applications (literal)
- Abstract
- An efficient N-selective alkylation of primary aromatic amines in molten quaternary ammonium salts, as the solvent, under relatively mild and base-free conditions is presented. On the basis of the KamletTaft parameters and the nucleophilicity of the IL (ionic liquid) anions, the influence of the ionic liquid was evaluated. This protocol was validated on a larger multigram scale and with the syntheses of bioactive heterocycles (e.g., 1,4-benzothiazine and quinoxalines) and new efficient MALDI matrixes. (literal)
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