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https://doi.org/10.1016/j.tetlet.2004.08.007
| Title: | Arylcarbamoylated allylcarbamido-β-cyclodextrin: Synthesis and immobilization on nonfunctionalized silica gel as a chiral stationary phase | Authors: | Bai, Z.-W. Lai, X.-H. Chen, L. Ching, C.-B. Ng, S.-C. |
Keywords: | Allylcarbamido-β-cyclodextrin Arylcarbamate Chiral stationary phase Enantioseparation Hydrosilylation Silanization |
Issue Date: | 20-Sep-2004 | Citation: | Bai, Z.-W., Lai, X.-H., Chen, L., Ching, C.-B., Ng, S.-C. (2004-09-20). Arylcarbamoylated allylcarbamido-β-cyclodextrin: Synthesis and immobilization on nonfunctionalized silica gel as a chiral stationary phase. Tetrahedron Letters 45 (39) : 7323-7326. ScholarBank@NUS Repository. https://doi.org/10.1016/j.tetlet.2004.08.007 | Abstract: | Four new chiral stationary phases based on mono-(6 A- allylcarbamido-6 A-deoxy)-arylcarbamoylated β-cyclodextrin were synthesized. The chiral stationary phase of phenylcarbamoylated β-cyclodextrin exhibited excellent separation capability for a variety of chiral compounds. Compared with previous work, it was found that the spacer remained on the surface of the silica gel and decreased the enantioseparation capability. © 2004 Elsevier Ltd. All rights reserved. | Source Title: | Tetrahedron Letters | URI: | http://scholarbank.nus.edu.sg/handle/10635/88556 | ISSN: | 00404039 | DOI: | 10.1016/j.tetlet.2004.08.007 |
| Appears in Collections: | Staff Publications |
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