“…Such a pattern is char acteristic of the formation of low polarity associates. 12, 15 The data obtained suggest that calix [4]resorcinols with acetal groups in the aminomethyl fragment, like their simpler aminomethylated analogs, 15 form head to head supramolecular aggregates in chloroform at low concen trations. 1.1 3,7 .1 9,13 .1 15,19 ]octacosa 1(25),3,5,7(28),9,11,13(27),15,17,19(26),21,23 dodecaene (3c) was obtained analogously from calixarene 1c (1.57 g, 2.4 mmol), acetal 2 (1.43 g, 12 mmol), and 30% formalin (1.20 g, 12 mmol 15,17,19(26),21,23 dodecaene (3e) was obtained analogously from calixarene 1e (5 g, 6.07 mmol), acetal 2 (3.61 g, 30.34 mmol), and 30% formalin (3.03 g, 30.34 mmol).…”