Abstract
AbstractA stable selenenic acid bearing a bridged calix[6]arene framework fixed in the 1,2,3‐alternate conformation was synthesized. Its properties were compared with those of its conformational isomer fixed in the cone conformation, indicating that the reactivity of the endohedral SeOH group can be regulated by the conformation of the calix[6]arene framework. © 2001 John Wiley & Sons, Inc. Heteroatom Chem 12:195–197, 2001
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