A facile synthesis of novel types of cyclodextrin derivatives by insertion of an aromatic dicarbonyl spacer into a permethylated α-cyclodextrin skeleton
A facile synthesis of novel types of cyclodextrin derivatives by insertion of an aromatic dicarbonyl spacer into a permethylated α-cyclodextrin skeleton
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DOI：
10.1039/b204960k
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发表时间：
2002-01-01
影响因子：
4.9
通讯作者：
Ikeda, I
中科院分区：
文献类型：
--
作者：
Kida, T;Michinobu, T;Ikeda, I
通过在全甲基化α-环糊精的骨架上插入一个芳香族二羰基间隔基，可以很容易地合成出新型的环糊精衍生物，并且插入间苯二甲酰的环糊精对对硝基苯酚的络合能力与全甲基化β-环糊精几乎相同。
Novel types of cyclodextrin derivatives are easily synthesized by the insertion of an aromatic dicarbonyl spacer into the skeleton of permethylated alpha-cyclodextrin, and the isophthaloyl-inserted one shows almost the same complexing ability toward p-nitrophenol as permethylated beta-cyclodextrin.