Issue 6, 1972

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 β-anomer has been converted into 1,2,3-triazole derivatives by reaction with benzyl azide.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 346-347

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 and M. J. Power, J. Chem. Soc., Chem. Commun., 1972, 346 DOI: 10.1039/C39720000346

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements