2021
DOI: 10.1016/j.talanta.2020.121987
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Preparation and applications of cellulose-functionalized chiral stationary phases: A review

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Cited by 45 publications
(23 citation statements)
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“…There are many hydroxyl groups at the C-2, C-3, and C-6 positions of the glucopyranose units that can be derivatized. Since Okamoto et al reported polysaccharide derivatives as attractive CSPs for HPLC in 1984 [23], many examples with different functional groups have been developed to prepare CSPs [41,42,111]. The polysaccharide phenylcarbamates exhibit outstanding chiral recognition performance.…”
Section: Cellulose and Amylose-based Cspsmentioning
confidence: 99%
See 1 more Smart Citation
“…There are many hydroxyl groups at the C-2, C-3, and C-6 positions of the glucopyranose units that can be derivatized. Since Okamoto et al reported polysaccharide derivatives as attractive CSPs for HPLC in 1984 [23], many examples with different functional groups have been developed to prepare CSPs [41,42,111]. The polysaccharide phenylcarbamates exhibit outstanding chiral recognition performance.…”
Section: Cellulose and Amylose-based Cspsmentioning
confidence: 99%
“…Although reviews of CSPs for HPLC have been published previously [41][42][43], they are all generally focused on one type of CSP. During the last 3 years, many researchers have made great efforts to develop novel CSPs for HPLC enantioseparation and a variety of new CSPs have been reported.…”
Section: Introductionmentioning
confidence: 99%
“…7,8 high-performance liquid chromatography (HPLC) using a chiral stationary phase (CSP) is generally recognized as one of the most popular and effective methods for both analytical and preparative purposes. [9][10][11][12][13][14][15][16][17] The key factor for chiral chromatographic separation is the development of novel CSPs with high enantioseparation ability. In the past decades, various effective CSPs…”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3][4] The biological activity of their enantiomers is remarkably different. [5][6][7] For example, (R)chloramphenicol is active, but (S)-chloramphenicol is inactive; (L)-dopa is used for the treatment of Parkinson's disease, but (D)dopa has serious side effects; (R)-thalidomide exerts a sedative and hypnotic effect, while (S)-thalidomide exerts immunosuppressive efficacy. [8][9][10][11] It is of necessity to evaluate drug safety and protect people's health through enantioseparation of drugs.…”
Section: Introductionmentioning
confidence: 99%