Synthesis of 2,3,5-tri-O-benzyl-α- (and β-)-D- ribofuranosylethyne, potential intermediates for the synthesis of C-nucleosides

J. G. Buchanan, A. R. Edgar, M. J. Power

Research output: Contribution to journalArticle

Abstract

Two methods are described for the synthesis of the anomers of 2,3,5-tri-O-benzyl-D-ribofuranosyelthyne; the ß-anomer has been converted into 1,2,3-triazole derivatives by reaction with benzyl azide.

Original languageEnglish
Pages (from-to)346-347
Number of pages2
JournalJournal of the Chemical Society, Chemical Communications
Volume0
Issue number6
DOIs
Publication statusPublished - 1972

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Triazoles
Azides
Nucleosides
Derivatives
2,3,5-tri-O-benzyl D-ribofuranosylethyne

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abstract = "Two methods are described for the synthesis of the anomers of 2,3,5-tri-O-benzyl-D-ribofuranosyelthyne; the {\ss}-anomer has been converted into 1,2,3-triazole derivatives by reaction with benzyl azide.",
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Synthesis of 2,3,5-tri-O-benzyl-α- (and β-)-D- ribofuranosylethyne, potential intermediates for the synthesis of C-nucleosides. / Buchanan, J. G.; Edgar, A. R.; Power, M. J.

In: Journal of the Chemical Society, Chemical Communications, Vol. 0, No. 6, 1972, p. 346-347.

Research output: Contribution to journalArticle

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