Selective O-functionalization of phenolic alpha-amino acids with crown ethers bearing cyclophosphazene sub-units (Articolo in rivista)

Type
Label
  • Selective O-functionalization of phenolic alpha-amino acids with crown ethers bearing cyclophosphazene sub-units (Articolo in rivista) (literal)
Anno
  • 2011-01-01T00:00:00+01:00 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
  • 10.1016/j.tet.2011.01.053 (literal)
Alternative label
  • Penso M.; Maia A.; Lupi V.; Tricarico G. (2011)
    Selective O-functionalization of phenolic alpha-amino acids with crown ethers bearing cyclophosphazene sub-units
    in Tetrahedron (Oxf., Print)
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Penso M.; Maia A.; Lupi V.; Tricarico G. (literal)
Pagina inizio
  • 2096 (literal)
Pagina fine
  • 2102 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
  • http://www.scopus.com/inward/record.url?eid=2-s2.0-79952039032&partnerID=q2rCbXpz (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
  • 67 (literal)
Rivista
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
  • 11 (literal)
Note
  • Scopu (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • CNR, Istituto di Scienze e Tecnologie Molecolari (ISTM), Via Golgi 19, I-20133 Milano, Italy; Dipartimento di Chimica Organica e Industriale dell'Universit, Via Venezian 21, I-20133 Milano, Italy; Nerviano Medical Sciences, Viale Pasteur 10, I-20014 Nerviano, Italy; Galapagos NV, Industriepark Mechelen Noord, Generaal De Wittelaan L11 A3, B-2800 Mechelen, Belgium (literal)
Titolo
  • Selective O-functionalization of phenolic alpha-amino acids with crown ethers bearing cyclophosphazene sub-units (literal)
Abstract
  • Cyclophosphazenes (CyP) containing a crown ether and an ?-amino acid unit have been prepared starting from diphosphaza[16]crown-6 (PNP16C6). Nucleophilic substitution of one (or both) residual ansa-chlorine atom(s) of bis-spiro substituted PNP16C6 by ?-arylsulfonamido esters containing a phenolic function leads to the target compounds. These new polyfunctionalized CyP are lariat ethers, potentially useful as starting materials for the preparation of 'pH-controlled active ion carriers' in liquid membranes. © 2011 Elsevier Ltd. All rights reserved. (literal)
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