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- W2135233602 abstract "1,3-Diether derivatives of tert-butylcalix[4]arene can be selectively nitrated at the para-position of the phenolic units. In this way clix[4]arenes bearing tert-butyl and nitro groups at the upper rim in alternating sequence are easily available in yields up to 75% Ipso-attack may also occur ortho to the phenolic hydroxy group leading in a side reaction to macrocyclic compounds with two 6-nitrocyclohexa-2,4-dienone units. Both types of structures were established by single crystal X-ray analysis." @default.
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- W2135233602 date "1996-01-01" @default.
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- W2135233602 title "Selective ipso-nitration of tert-butylcalix[4]arene 1,3-diethers: X-ray structure of an unexpected side product" @default.
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- W2135233602 doi "https://doi.org/10.1039/p19960001711" @default.
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