http://www.cnr.it/ontology/cnr/individuo/prodotto/ID48392

Oxazoline-containing phosphazene derivatives. Parte III. Synthesis and characterization of novel cyclophosphazenes functionalized with chiral 2-oxazoline groups. (Articolo in rivista)

Type

Label

Oxazoline-containing phosphazene derivatives. Parte III. Synthesis and characterization of novel cyclophosphazenes functionalized with chiral 2-oxazoline groups. (Articolo in rivista) (literal)

Anno

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi

Alternative label

1-Fiocca L.; 1-Po' R.; 1-Giannotta G.; 2-Gleria M.; 2-Venzo A.; 3-Milani R.; 3-De Paoli G. (2008)
Oxazoline-containing phosphazene derivatives. Parte III. Synthesis and characterization of novel cyclophosphazenes functionalized with chiral 2-oxazoline groups.
in Designed monomers and polymers (Print); Brill Academic Publishers, Leiden (Paesi Bassi)
(literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori

1-Fiocca L.; 1-Po' R.; 1-Giannotta G.; 2-Gleria M.; 2-Venzo A.; 3-Milani R.; 3-De Paoli G. (literal)

Pagina inizio

Pagina fine

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume

Rivista

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali

Note

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni

1-ENI SpA-Divisione Refining and Marketing, Centro Ricerche Novara, Via G. Fauser 4, 28100 Novara, Italy 2-ISTM-CNR, Via Marzolo 1, 35131 Padova, Italy 3-Dipartimento di Scienze Chimiche dell'Università, Via F. Marzolo 1, 35131 Padova, Italy (literal)

Titolo

Oxazoline-containing phosphazene derivatives. Parte III. Synthesis and characterization of novel cyclophosphazenes functionalized with chiral 2-oxazoline groups. (literal)

Abstract

In this paper we describe the synthesis and the characterization of a series of cyclophosphazenes substituted with 2-oxazoline-containing moieties, with and without optical activity. These products could be obtained by reacting cyclophosphazenes containing six (hexachlorocyclophosphazene, C-6-Cl), two (2,2-dichloro-4,4,6,6-bis[spiro(2',2''-dioxy-1',1''-biphenyl)]cyclophosphazene, C-2-Cl) and one (pentakis(phenoxy)monochlorocyclophosphazene, C-1-Cl) chlorine atoms, respectively, with a series of 4-hydroxyphenyl-2-oxazolines, as obtained by condensation reaction of methyl-4-hydroxybenzoate with 2-aminoethanol and with chiral and racemic 1-amino-2-propanol, and successive cyclization reactions of the resulting hydroxyamides to 2-oxazoline compounds. (literal)

Editore