Synthesis of symmetrically modified α-cyclodextrins:: an efficient and easy method

被引:19
作者
Heck, R
Jicsinszky, L
Marsura, A
机构
[1] UHP, GEVSM, Fac Pharm, CNRS,UMR 7565, F-54001 Nancy, France
[2] Cyclolab Ltd, H-1525 Budapest, Hungary
关键词
D O I
10.1016/S0040-4039(03)01313-3
中图分类号
O62 [有机化学];
学科分类号
070303 [有机化学]; 081704 [应用化学];
摘要
Efficient and simple synthetic methods of designed specific synthons of cyclodextrins are fundamental for the further development of more sophisticated supramolecular devices. Here, a new two step synthesis was proposed for the obtention of the 6(A),6(C),6(E)-triazido-6(A),6(C),6(E)-trideoxy-6(B),6(D),6(F)-tri-O-methylhexakis-(2,3-di-O-methyl)cyclomaltohexaose on a large scale. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:5411 / 5413
页数:3
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