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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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Differential and substrate-selective reactivity of calix[4]arene derivatives with cyclenyl-Zn(II) modifications at the upper rim.

[structure: see text] Novel "cone conformation" calix[4]arene derivatives, carrying either one or two cyclen (1,4,7,10-tetra-azacyclododecane) moieties at the upper rim, have been synthesized. The hydrolytic activities of the Zn(II) complexes of these calixarenes were studied. A surprising behavior was observed with p-nitrophenylstearate; whereas the bis-cyclenyl-2Zn(II) complex showed negligible hydrolytic activity over the background, the mononuclear complex showed a significant 400-fold rate increase at pH 8.5.[1]

References

  1. Differential and substrate-selective reactivity of calix[4]arene derivatives with cyclenyl-Zn(II) modifications at the upper rim. Ozturk, G., Akkaya, E.U. Org. Lett. (2004) [Pubmed]
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