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Titolo:
A NEWLY DEVISED METHOD FOR THE DEBENZYLATION OF N-6-BENZYLADENOSINES - A CONVENIENT SYNTHESIS OF [6-N-15]-LABELED ADENOSINES
Autore:
SAKO M; ISHIKURA H; HIROTA K; MAKI Y;
Indirizzi:
GIFU PHARMACEUT UNIV,MED CHEM LAB,6-1 MITAHORA HIGASHI 5 CHOME GIFU 502 JAPAN
Titolo Testata:
Nucleosides & nucleotides
fascicolo: 6-7, volume: 13, anno: 1994,
pagine: 1239 - 1246
SICI:
0732-8311(1994)13:6-7<1239:ANDMFT>2.0.ZU;2-K
Fonte:
ISI
Lingua:
ENG
Soggetto:
N-15 NMR-SPECTROSCOPY; NITROGEN-15-LABELED OLIGODEOXYNUCLEOTIDES; ADENINE N1; BINDING; DEOXYADENOSINE; DERIVATIVES; CONVERSION; SECONDARY; ANALOGS; ATP;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Science Citation Index Expanded
Citazioni:
26
Recensione:
Indirizzi per estratti:
Citazione:
M. Sako et al., "A NEWLY DEVISED METHOD FOR THE DEBENZYLATION OF N-6-BENZYLADENOSINES - A CONVENIENT SYNTHESIS OF [6-N-15]-LABELED ADENOSINES", Nucleosides & nucleotides, 13(6-7), 1994, pp. 1239-1246

Abstract

[6-N-15]-Labeled adenosine was conveniently prepared from inosine (1a) by the silylation-benzylamination of 1a and subsequent oxidative debenzylation with ammonium peroxydisulfate in a pH 7.2 buffer solution.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 15/07/20 alle ore 14:58:21