An efficient synthesis of 7-functionalized 7-deazapurine beta-D-or beta-L-ribonucleosides: Glycosylation of pyrrolo[2,3-d]pyrimidines with 1-O-acetyl-2,3,5-tri-O-benzoyl-D- or L-ribofuranose

Autor(en): Peng, Xiaohua
Seela, Frank
Stichwörter: 7-deazapurines; Biochemistry & Molecular Biology; functionalization; glycosylation; NUCLEOSIDES; pyrrolo[2,3-d]pyrimidines; ribonucleosides; Silyl Hilbert-Johnson reaction
Erscheinungsdatum: 2007
Herausgeber: TAYLOR & FRANCIS INC
Journal: NUCLEOSIDES NUCLEOTIDES & NUCLEIC ACIDS
Volumen: 26
Ausgabe: 6-7
Startseite: 603
Seitenende: 606
Zusammenfassung: 
The glycosylation reaction performed with 7-halogenated 7-deazapurines employing commercially available 1-O-acetyl-2,3,5-tri-O-benzoyl-D-or L-ribofuranoses is described.
Beschreibung: 
Proceedings of the 17th International Roundtable of Nucleosides, Nucleotides, and Nucleic Acids, Bern, SWITZERLAND, MAR 07-SEP 07, 2006
ISSN: 15257770
DOI: 10.1080/15257770701490332

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