Catalogo Articoli (Spogli Riviste)

OPAC HELP

Titolo:
Solid phase synthesis of carbocyclic L-2 '-deoxynucleosides
Autore:
Choo, H; Chong, YH; Chu, CK;
Indirizzi:
Univ Georgia, Coll Pharm, Dept Pharmaceut & Biomed Sci, Athens, GA 30602 USA Univ Georgia Athens GA USA 30602 aceut & Biomed Sci, Athens, GA 30602 USA
Titolo Testata:
ORGANIC LETTERS
fascicolo: 10, volume: 3, anno: 2001,
pagine: 1471 - 1473
SICI:
1523-7060(20010517)3:10<1471:SPSOCL>2.0.ZU;2-Z
Fonte:
ISI
Lingua:
ENG
Soggetto:
ASYMMETRIC-SYNTHESIS; NUCLEOSIDES; PYRIMIDINES; ANALOGS;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Physical, Chemical & Earth Sciences
Citazioni:
16
Recensione:
Indirizzi per estratti:
Indirizzo: Chu, CK Univ Georgia, Coll Pharm, Dept Pharmaceut & Biomed Sci, Athens, GA30602 USA Univ Georgia Athens GA USA 30602 Biomed Sci, Athens, GA 30602 USA
Citazione:
H. Choo et al., "Solid phase synthesis of carbocyclic L-2 '-deoxynucleosides", ORG LETT, 3(10), 2001, pp. 1471-1473

Abstract

[GRAPHICS]Carbocyclic L-2 ' deoxynucleosides 17 were synthesized on solid phase in four steps from the appropriately protected intermedate 11, The Mitsunobu reaction was used as a condensation method between the carbocyclic moiety andheterocyclic bases. The regioselectivity of the carbocyclic nucleosides was compared between the solid and solution phase syntheses.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 24/10/20 alle ore 14:43:16