Synthesis and Protonation Constants of an Amide-Based Chelating Cyclophane
Excerpt
Our research group have reported that, under high dilution conditions, condensation reactions between 4,4’-ethylenebis(2,6-morpholinedione), 1, and aromatic diamines gave a new series of tetraaza chelating cylophanes, which have amide and aromatic groups in the ring framework and pendant carboxymethyl groups [1].[...] View Full-TextSupplementary materials
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3D structure generated by CORINA by Molecular Networks. - Supplementary File 2:
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Altamirano-Coronado, J.C.; Godoy-Alcántar, C.; Medrano, F. Synthesis and Protonation Constants of an Amide-Based Chelating Cyclophane. Molbank 2006, 2006, M519.
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