A series of C 3 -symmetric tris(3,5-dialkyl-2-hydroxyphenyl)-methanes (alkyl = tert-butyl, methyl, tert-pentyl) have been synthesized in high yield from their respective phenols and fully characterized, including single crystal X-ray structures for two examples. The di-tert-butyl-substituted compound, 1a, has been derivatized to a tris-acid chloride, 4, which was treated with a variety of amines (dimethylamine, benzylamine, glycine, and alanine) from which the corresponding trisamides 5−8 were formed. The absolute geometry and conformation of the dimethylamine, glycine, and alanine derived systems were determined by X-ray analyses, and in all cases,