Tris(3,5-dialkyl-2-hydroxyphenyl)methanes (tert-butyl, tert-pentyl) react with three equivalents of sodium hydride to give hexanuclear dimers; these bulky aggregates have six well-defined coordination ‘pockets’ which demonstrate selectivity toward a variety of ketones.
M. B. Dinger and M. J. Scott, Chem. Commun., 1999, 2525 DOI: 10.1039/A907476G
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