The new macrocyclic molecule 19 shows dramatically improved solubility in methanol
A general and high yielding fragment coupling synthesis of heteroatom-bridged calixarenes and the unprecedented examples of calixarene cavity fine-tuned by bridging heteroatoms
Scheme 5
In the presence of diisopropylethylamine, for example, diazadioxocalix[2]arene[2]triazine 9 underwent an efficient nucleophilic substitution reaction with diethanolamine to furnish product 19 in 72% yield. Having been functionalized with four hydroxy groups, the new macrocyclic molecule 19 shows dramatically improved solubility in methanol (Scheme 5).
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