Selective mono- and 1,4-di-N-alkylations of 1,4,7,10-tetraazacyclododecane

17Citations
Citations of this article
7Readers
Mendeley users who have this article in their library.

Abstract

General methods for selective N-alkylations of the macrocycle 1,4,7,10-tetraazacyclododecane have been developed. The N-monoalkylation proceeds via a cyclic guanidinium derivative, and the rcgioseleclive 1,4-N,N-dialkylation via a cyclic amidinium derivative. All transformations were high yield reactions. © Acta Chemica Scandinavica 1998.

Cite

CITATION STYLE

APA

Li, Z., & Undheim, K. (1998). Selective mono- and 1,4-di-N-alkylations of 1,4,7,10-tetraazacyclododecane. Acta Chemica Scandinavica, 52(10), 1247–1253. https://doi.org/10.3891/acta.chem.scand.52-1247

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free