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Titolo:
Photochemical synthesis of novel dideoxynucleosides
Autore:
Lee-Ruff, E; Margau, R;
Indirizzi:
York Univ, Dept Chem, Toronto, ON M3J 1P3, Canada York Univ Toronto ON Canada M3J 1P3 ept Chem, Toronto, ON M3J 1P3, Canada
Titolo Testata:
NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS
fascicolo: 3, volume: 20, anno: 2001,
pagine: 185 - 196
SICI:
1525-7770(2001)20:3<185:PSOND>2.0.ZU;2-M
Fonte:
ISI
Lingua:
ENG
Soggetto:
ISOMERIC DIDEOXYNUCLEOSIDES; NUCLEOSIDES; ANALOGS; APIOSE;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Life Sciences
Citazioni:
23
Recensione:
Indirizzi per estratti:
Indirizzo: Lee-Ruff, E York Univ, Dept Chem, Toronto, ON M3J 1P3, Canada York Univ Toronto ON Canada M3J 1P3 ronto, ON M3J 1P3, Canada
Citazione:
E. Lee-Ruff e R. Margau, "Photochemical synthesis of novel dideoxynucleosides", NUCLEOS NUC, 20(3), 2001, pp. 185-196

Abstract

A series of 2 ' ,3 ' -dideoxynucleosides based on the apiose family was prepared from photochemical ring-expansion of a common cyclobutanone precursor. The starting ketone, (+/-) 3-[2 '-(benzoyloxy)ethyl]-2,2-dimethylcyclobutanone (12) was prepared from commercially available (+/-)alpha -pinene. Since the optically pure antipodes of alpha -pinene are also commercially available, these nucleosides can be prepared optically pure using the identical procedure.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 19/01/20 alle ore 01:20:25