Abe Hajime, Aoyagi Yoshinobu, Inouye Masahiko
Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University, Toyama, 930-0194 Japan.
Org Lett. 2005 Jan 6;7(1):59-61. doi: 10.1021/ol047907c.
A rigid C(3v)-symmetrical host molecule, syn-1,3,5-tris(2-hydroxy-5-pentylphenyl)-2,4,6-trimethylbenzene, was readily obtained via Suzuki coupling and thermal atropisomerization. The host molecule effectively associated with various saccharides by multipoint hydrogen bonds, whereas its anti-atropisomer and analogue lacking in methyl groups showed much weaker association with saccharides. Thermodynamic analyses suggested that the difference of the association strength was caused by entropic factors.
一种刚性的具有C(3v)对称性的主体分子,即顺式-1,3,5-三(2-羟基-5-戊基苯基)-2,4,6-三甲基苯,通过铃木偶联反应和热轴手性异构化反应可轻松制得。该主体分子通过多点氢键与各种糖类有效结合,而其反式轴手性异构体及缺乏甲基的类似物与糖类的结合则弱得多。热力学分析表明,结合强度的差异是由熵因素引起的。