Issue 6, 1975

A convenient synthesis of the tetra-aza-macrocyclic ligands trans-[14]-diene, tet a, and tet b

Abstract

A convenient synthesis of 5,7,7,12,14,14-hexamethyl-1,4,8,11-tetra-azacyclotetradeca-4,11-diene (trans-[14]diene) is described. Reduction with sodium borohydride gives the two diastereoisomeric 5,7,7,12,14,14-hexamethyl-1,4,8,11-tetra-azacyclotetradecanes, tet a and tet b, which are readily separated.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1975, 591-593

A convenient synthesis of the tetra-aza-macrocyclic ligands trans-[14]-diene, tet a, and tet b

R. W. Hay, G. A. Lawrance and N. F. Curtis, J. Chem. Soc., Perkin Trans. 1, 1975, 591 DOI: 10.1039/P19750000591

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