Issue 12, 1981

Cu2+-promoted Hydrolysis of cyanomethyl-substituted tetra-azamacrocycles

Abstract

The fast Cu2+-promoted hydrolysis of the two macrocyclic nitriles (3) and (4) is due to the proximity of the reactants allowing an intramolecular nucleophilic attack of the co-ordinated OH on the cyano-group to take place.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1981, 603-604

Cu2+-promoted Hydrolysis of cyanomethyl-substituted tetra-azamacrocycles

W. Schibler and T. A. Kaden, J. Chem. Soc., Chem. Commun., 1981, 603 DOI: 10.1039/C39810000603

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