Issue 15, 1975

Synthesis of nucleosides by direct replacement of the anomeric hydroxy-group

Abstract

A novel synthesis of purine nucleosides of aldoses and ketoses has been developed, by a method involving treatment of an appropriately protected sugar derivative having a free anomeric hydroxy-group with 6-chloropurine, diethyl azodicarboxylate, and methyldiphenylphosphine.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1975, 648-649

Synthesis of nucleosides by direct replacement of the anomeric hydroxy-group

W. A. Szarek, C. Depew, H. C. Jarrell and J. K. N. Jones, J. Chem. Soc., Chem. Commun., 1975, 648 DOI: 10.1039/C39750000648

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