Issue 7, 1994

New general synthesis of organophosphorus P–F compounds via reaction of azolides of phosphorus acids with acyl fluorides: novel route to 2-deoxynucleosidyl phosphorofluoridates and phosphorodifluoridates

Abstract

Tetra- and tri-coordinate P–N-imidazole derivatives and their structural analogues react smoothly with acyl fluorides to give the corresponding P–F compounds in almost quantitative yield. This method has been successfully applied to produce 2-deoxynucleosidyl phosphorofluoridates and phosphorodifluoridates.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1994, 817-820

New general synthesis of organophosphorus P–F compounds via reaction of azolides of phosphorus acids with acyl fluorides: novel route to 2-deoxynucleosidyl phosphorofluoridates and phosphorodifluoridates

W. Dąbkowski, J. Michalski, J. Wasiak and F. Cramer, J. Chem. Soc., Perkin Trans. 1, 1994, 817 DOI: 10.1039/P19940000817

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