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.
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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
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