The synthesis of oligoribonucleotides. III. The use of silyl protecting groups in nucleoside and nucleotide chemistry. VIII

The synthesis of all isomeric mono- and disilyl derivatives of cytidine, guanosine, and their N-benzoyl analogues using the tert-butyldimethylsilyl protecting group is described. These compounds and those containing a 5′-monomethoxytrityl group have been condensed via the phosphodichloridite procedu...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Canadian journal of chemistry 1979-09, Vol.57 (17), p.2230-2238
Hauptverfasser: Ogilvie, Kelvin K, Schifman, Aria L, Penney, Christopher L
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The synthesis of all isomeric mono- and disilyl derivatives of cytidine, guanosine, and their N-benzoyl analogues using the tert-butyldimethylsilyl protecting group is described. These compounds and those containing a 5′-monomethoxytrityl group have been condensed via the phosphodichloridite procedure to produce nucleotides rapidly and in good yields. The synthesis of 2′-5′-linked nucleotides is described. A cautionary note is introduced in regard to the preparation of 5′-monomethoxytritylguanosine and a novel methanolysis of certain N-benzoylcytidines is mentioned.
ISSN:0008-4042
1480-3291
DOI:10.1139/v79-357