http://www.cnr.it/ontology/cnr/individuo/prodotto/ID48595
Selective O-functionalization of phenolic a-amino acids with crown ethers bearing cyclophosphazene sub-units (Articolo in rivista)
- Type
- Label
- Selective O-functionalization of phenolic a-amino acids with crown ethers bearing cyclophosphazene sub-units (Articolo in rivista) (literal)
- Anno
- 2011-01-01T00:00:00+01:00 (literal)
- Alternative label
Penso, Michele; Maia, Angelamaria; Lupi, Vittoria; Tricarico, Giovanni (2011)
Selective O-functionalization of phenolic a-amino acids with crown ethers bearing cyclophosphazene sub-units
in Tetrahedron (Oxf., Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Penso, Michele; Maia, Angelamaria; Lupi, Vittoria; Tricarico, Giovanni (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#note
- doi:10.1016/j.tet.2011.01.053 (literal)
- Note
- ISI Web of Science (WOS) (literal)
- Titolo
- Selective O-functionalization of phenolic a-amino acids with crown ethers bearing cyclophosphazene sub-units (literal)
- Abstract
- Cyclophosphazenes (CyP) containing a crown ether and an a-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 a-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. (literal)
- Prodotto di
- Autore CNR
Incoming links:
- Prodotto
- Autore CNR di
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#rivistaDi