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Dicationic AC regioisomer cyclodextrins: mono-6A-ammonium-6C-alkylimidazolium-β-cyclodextrin chlorides as chiral selectors for enantioseparation
| Content Provider | Semantic Scholar |
|---|---|
| Author | Wang, Shuye Wu, Jian-Hua Tang, Jian Tang, Weihua |
| Copyright Year | 2012 |
| Abstract | Dicationic cyclodextrins with AC regioisomer structure were prepared by monosubstitution of 6A-azido-β-cyclodextrin with 2-mesitylenesulfonyl chloride and the Staudinger reaction. One family of the desired cyclodextrins, the 6A-ammonium-6C-butylimidazolium-β-cyclodextrin chlorides, demonstrated a good chiral recognition ability towards both acidic and even neutral racemates even at concentrations as low as 0.5 mM. |
| Starting Page | 12652 |
| Ending Page | 12656 |
| Page Count | 5 |
| File Format | PDF HTM / HTML |
| DOI | 10.1039/C2RA21940A |
| Alternate Webpage(s) | http://www.rsc.org/suppdata/ra/c2/c2ra21940a/c2ra21940a.pdf |
| Alternate Webpage(s) | https://doi.org/10.1039/C2RA21940A |
| Volume Number | 2 |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |