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

doi:10.1039/C39720000346

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

School of Engineering & Physical Sciences

Research output: Contribution to journal › Article › peer-review

16 Citations (Scopus)

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 language	English
Pages (from-to)	346-347
Number of pages	2
Journal	Journal of the Chemical Society, Chemical Communications
Volume	0
Issue number	6
DOIs	https://doi.org/10.1039/C39720000346
Publication status	Published - 1972

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

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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AU - Edgar, A. R.

AU - Power, M. J.

PY - 1972

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AB - 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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DO - 10.1039/C39720000346

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JO - Journal of the Chemical Society, Chemical Communications

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ER -

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

Abstract

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