Issue 18, 1991

Highly regioselective synthesis of 1,7-diprotected 1,4,7,10-tetraazacyclododecane derivatives

Abstract

Reaction of dimethylformamicle diethyl acetal with monoalkylated 1,4,7,10-tetraazacyclododecane derivatives 3, followed by hydrolysis of the tricyclic intermediates 4, selectively affords 1,7-disubstituted tetraazamacrocycles 5.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1991, 1317-1318

Highly regioselective synthesis of 1,7-diprotected 1,4,7,10-tetraazacyclododecane derivatives

P. L. Anelli, M. Murru, F. Uggeri and M. Virtuani, J. Chem. Soc., Chem. Commun., 1991, 1317 DOI: 10.1039/C39910001317

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