N, N′-bis(dichloro-s-triazinyl)-m-phe- nylenediamine 11 underwent macrocyclizative coupling reactions
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 2
Being a reactive intermediate, N, N′-bis(dichloro-s-triazinyl)-m-phe- nylenediamine 11 underwent macrocyclizative coupling reactions with 3-aminophenol 4 and m-phenylenediamines 5 and 6 to produce the desired hetereoatom-bridged calix[2]arene[2]-triazines 12, 13,20 and 14 in 46-58% yields (Scheme 2).
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