Syntheses of chiral calixarene analog incorporating amino acid residues: Molecular recognition for a racemic ammonium ion by the macrocycles

被引：28

作者：

Ito, K ^{[1
]}

Kida, A ^{[1
]}

Ohba, Y ^{[1
]}

Sone, T ^{[1
]}

机构：

[1] Yamagata Univ, Fac Engn, Dept Mat Sci & Engn, Yonezawa, Yamagata 9920038, Japan

来源：

CHEMISTRY LETTERS | 1998年 / 12期

关键词：

D O I：

10.1246/cl.1998.1221

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Chiral calixarene analog incorporating amino acid residues into macrocyclic rings was prepared. The macrocycles form a chiral concave, which is induced by the chiral transmission from the amino acid to the phenol-formaldehyde tetramer unit through the hydrogen bonds. Molecular recognition for a chiral ammonium ion by the macrocycles was investigated.

引用

页码：1221 / 1222

页数：2

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