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Dimercuration of Calix[4]arenes: Novel Substitution Pattern in Calixarene Chemistry

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https://figshare.com/articles/dataset/Dimercuration_of_Calix_4_arenes_Novel_Substitution_Pattern_in_Calixarene_Chemistry/2336530
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A mercuration reaction of tetrapropoxycalix[4]­arene immobilized in the cone conformation gave a mixture of two dimercurated products (meta,meta and meta,para) in approximately a 1:1 ratio. Both regioisomers represent inherently chiral compounds, which makes them very attractive for design of novel receptors. As demonstrated by Pd-catalyzed arylation, the different reactivity of HgCl functions in the meta,para-disubstituted isomer opens the door for regioselective introductions of two different functional groups to achieve a substitution pattern so far unknown in calixarene chemistry.
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2016-02-18
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