Issue 12, 2012
From the journal:

RSC Advances

Monosubstituted dually cationic cyclodextrins for stronger chiral recognition†

Jie Zhou,‡a   Yun Dai,‡a   Shuye Wang,a   Enwei Zhu,a   Jiefeng Hai,a   Yun Liu,a   Jian Tang*a  and  Weihua Tang*a  

* Corresponding authors

a Key Laboratory of Soft Chemistry and Functional Materials, Ministry of Education, Nanjing University of Science and Technology, Nanjing, P. R. China.
E-mail: tangj2005@hotmail.com, whtang@mail.njust.edu.cn
Fax: +86 25 8431 7311
Tel: +86 25 8431 7311

Abstract

Novel monosubstituted dually cationic cyclodextrins (CDs) have been synthesized by anchoring different alkyl chain spaced imidazolium and ammonium sidearm onto the CD primary ring. These cationic CDs exhibit satisfactory enantioselectivities for amino acids and acidic racemates in aqueous capillary electrophoresis.

Graphical abstract: Monosubstituted dually cationic cyclodextrins for stronger chiral recognition

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Article information

DOI
https://doi.org/10.1039/C2RA20086D
Article type
Communication
Submitted
15 Jan 2012
Accepted
10 Mar 2012
First published
13 Mar 2012

RSC Adv., 2012,2, 5088-5093

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Monosubstituted dually cationic cyclodextrins for stronger chiral recognition

J. Zhou, Y. Dai, S. Wang, E. Zhu, J. Hai, Y. Liu, J. Tang and W. Tang, RSC Adv., 2012, 2, 5088 DOI: 10.1039/C2RA20086D

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