Synthesis of 5-aza-7-deazapurine and 3,7-dideazapurine 2'-deoxyribofuranosides by solid-liquid phase-transfer glycosylation.

Autor(en): Seela, F.
Rosemeyer, H. 
Bourgeois, W.
Stichwörter: Deoxyribonucleosides; Glycosides; Indicators and Reagents; Purine Nucleosides; deoxyribonucleoside; dyes, reagents, indicators, markers and buffers; glycoside; purine nucleoside, article; chemistry; synthesis, Chemistry; Deoxyribonucleosides; Glycosides; Indicators and Reagents; Purine Nucleosides
Erscheinungsdatum: 1987
Journal: Nucleic acids symposium series
Ausgabe: 18
Startseite: 49
Seitenende: 52
Zusammenfassung: 
The 2'-deoxyguanosine isostere 1 as well as the pyrrolo [3,2-c] pyridine 2'-deoxyribofuranosides 2a,b and 3a-d have been synthesized in high yield by solid-liquid phase-transfer glycosylation. It was shown that only the strongly nucleophilic pyrrolo [3,2-c] pyridines formed exclusively beta-2'-deoxyribofuranosides, whereas weakly nucleophilic imidazo [1,2-a]-s-triazines gave mixtures of anomers.
ISSN: 02613166
Externe URL: https://www.scopus.com/inward/record.uri?eid=2-s2.0-0023464953&partnerID=40&md5=d2c5d1a2bef9d8b6cafbccacd771f98f

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