Issue 0, 1970

Aminolysis of N-phosphorylated pyridines

Abstract

The reactivities of amines towards the N-phosphorylpyridinium ions are weakly dependent on the basicities of the amines, but other features of amine structure are important. It is argued that the transition states for displacement reactions at the phosphorus atom of phosphate derivatives have the pentaoxyphosphorane structure.

Article information

Article type
Paper

J. Chem. Soc. B, 1970, 53-57

Aminolysis of N-phosphorylated pyridines

G. W. Jameson and J. M. Lawlor, J. Chem. Soc. B, 1970, 53 DOI: 10.1039/J29700000053

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