Please use this identifier to cite or link to this item: 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
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