Bis-β-cyclodextrinyl- and bis-cellobiosyl-diazacrowns: synthesis and molecular complexation behaviors toward Busulfan anticancer agent and two basic aminoacids

被引:19
作者
Porwanski, Stanislaw [2 ]
Florence, Dumarcay-Charbonnier B. [1 ]
Menuel, Stephane [1 ]
Joly, Jean-Pierre [3 ]
Bulach, Veronique [4 ]
Marsurab, Alain [1 ]
机构
[1] Nancy Univ, Fac Pharm, UMR CNRS, F-54001 Nancy, France
[2] Univ Lodz, Dept Organ & Appl Chem, PL-90136 Lodz, Poland
[3] Nancy Univ, Fac Pharm, UMR CNRS, F-54506 Vandoeuvre Les Nancy, France
[4] Univ Strasbourg, Chim Coordinat Organ Lab, Int Ctr Frontier Res Chem, Inst Le Bel, F-67000 Strasbourg, France
关键词
D O I
10.1016/j.tet.2009.05.057
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The one-step synthesis of two C-2-symmetric receptors including two beta-cyclodextrin cores or two disaccharidyl units connected by urea linkers to a diazacrown ether organizing platform is reported. The X-ray structure of the peracetylated bis-ureidocellobiosyl podand could be determined. These molecular systems, long thought to be potent selective carriers for chiral/achiral organic guests at the supramolecular level, were found to be efficient complexing tools toward the Busulfan anticancer agent but also toward L-arginine and L-lysine basic aminoacids. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6196 / 6203
页数:8
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