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129 related items for PubMed ID: 23890199
1. Green synthesis of a typical chiral stationary phase of cellulose-tris(3, 5-dimethylphenylcarbamate). Liu RQ, Bai LY, Zhang YJ, Zhang YP. Chem Cent J; 2013 Jul 26; 7(1):129. PubMed ID: 23890199 [Abstract] [Full Text] [Related]
2. Synthesis of cellulose-2,3-bis(3,5-dimethylphenylcarbamate) in an ionic liquid and its chiral separation efficiency as stationary phase. Liu R, Zhang Y, Bai L, Huang M, Chen J, Zhang Y. Int J Mol Sci; 2014 Apr 11; 15(4):6161-8. PubMed ID: 24733066 [Abstract] [Full Text] [Related]
3. Enantioseparation Using Cellulose Tris(3,5-dimethylphenylcarbamate) as Chiral Stationary Phase for HPLC: Influence of Molecular Weight of Cellulose. Okada Y, Yamamoto C, Kamigaito M, Gao Y, Shen J, Okamoto Y. Molecules; 2016 Nov 08; 21(11):. PubMed ID: 27834832 [Abstract] [Full Text] [Related]
4. Direct enantiomeric resolutions of chiral triazole pesticides by high-performance liquid chromatography. Wang P, Jiang S, Liu D, Wang P, Zhou Z. J Biochem Biophys Methods; 2005 Mar 31; 62(3):219-30. PubMed ID: 15733582 [Abstract] [Full Text] [Related]
5. Nanocellulose 3, 5-Dimethylphenylcarbamate Derivative Coated Chiral Stationary Phase: Preparation and Enantioseparation Performance. Zhang X, Wang L, Dong S, Zhang X, Wu Q, Zhao L, Shi Y. Chirality; 2016 May 31; 28(5):376-81. PubMed ID: 26949227 [Abstract] [Full Text] [Related]
6. HPLC with cellulose Tris (3,5-DimethylPhenylcarbamate) chiral stationary phase: Influence of coating times and coating amount on chiral discrimination. Wei Q, Su H, Gao D, Wang S. Chirality; 2019 Mar 31; 31(3):164-173. PubMed ID: 30633381 [Abstract] [Full Text] [Related]
7. [Chiral separation of racemic epoxiconazole on cellulose tris(3,5-dimethylphenylcarbamate) chiral stationary phase using high performance liquid chromatography]. Han X, Wei Y, Liu Y, Chang J, Qiu W, Chen F. Se Pu; 2008 Sep 31; 26(5):631-3. PubMed ID: 19160767 [Abstract] [Full Text] [Related]
8. Chiral stationary phases based on chitosan bis(methylphenylcarbamate)-(isobutyrylamide) for high-performance liquid chromatography. Tang S, Bin Q, Chen W, Bai ZW, Huang SH. J Chromatogr A; 2016 Apr 01; 1440():112-122. PubMed ID: 26931425 [Abstract] [Full Text] [Related]
9. Fabrication of cellulose derivative coated spherical covalent organic frameworks as chiral stationary phases for high-performance liquid chromatographic enantioseparation. Yan YL, Guo D, Wu JL, Tang XH, Luo JJ, Li SQ, Fan J, Zheng SR, Zhang WG, Cai SL. J Chromatogr A; 2022 Jul 19; 1675():463155. PubMed ID: 35635867 [Abstract] [Full Text] [Related]
10. Comparative enantioseparation of seven triazole fungicides on (S,S)-Whelk O1 and four different cellulose derivative columns. Pan CX, Shen BC, Xu BJ, Chen JJ, Xu XZ. J Sep Sci; 2006 Aug 19; 29(13):2004-11. PubMed ID: 17017013 [Abstract] [Full Text] [Related]
11. Controlled synthesis, immobilization and chiral recognition of carboxylic acid functionalized cellulose tris(3,5-dimethylphenylcarbamate). Han M, Jin X, Yang H, Liu X, Liu Y, Ji S. Carbohydr Polym; 2017 Sep 15; 172():223-229. PubMed ID: 28606529 [Abstract] [Full Text] [Related]
12. The chiral separation of triazole pesticides enantiomers by amylose-tris (3,5-dimethylphenylcarbamate) chiral stationary phase. Wang P, Liu D, Jiang S, Xu Y, Zhou Z. J Chromatogr Sci; 2008 Oct 15; 46(9):787-92. PubMed ID: 19007480 [Abstract] [Full Text] [Related]
13. Direct optical resolution of the enantiomers of novel chiral tetrahedral metal clusters by HPLC on a cellulose tris-(3,5-dimethylphenylcarbamate) stationary phase. Li W, Zhang W, Zhao Q, Li Y, Ma C, Chen L, Yin Y. Anal Bioanal Chem; 2004 Mar 15; 378(5):1364-8. PubMed ID: 14735279 [Abstract] [Full Text] [Related]
14. Enantiomeric resolution of new triazole compounds by high-performance liquid chromatography. Lv C, Jia G, Zhu W, Qiu J, Wang X, Zhou Z. J Sep Sci; 2007 Feb 15; 30(3):344-51. PubMed ID: 17396592 [Abstract] [Full Text] [Related]
15. Chiral stationary phase based on cellulose derivative coated polymer microspheres and its separation performance. Li L, Yuan XT, Shi ZG, Xu LY. J Chromatogr A; 2020 Jul 19; 1623():461154. PubMed ID: 32505273 [Abstract] [Full Text] [Related]
16. [Homogeneous synthesis of cellulose phenylcarbamates and evaluation of their enantioseparation capabilities]. Yin C, Yang T, Zhang J, Zhang J. Se Pu; 2020 Apr 08; 38(4):476-483. PubMed ID: 34213231 [Abstract] [Full Text] [Related]
17. Reversed-phase chiral HPLC and LC/MS analysis with tris(chloromethylphenylcarbamate) derivatives of cellulose and amylose as chiral stationary phases. Peng L, Jayapalan S, Chankvetadze B, Farkas T. J Chromatogr A; 2010 Oct 29; 1217(44):6942-55. PubMed ID: 20863505 [Abstract] [Full Text] [Related]
18. Enantioseparations in nonaqueous capillary liquid chromatography and capillary electrochromatography using cellulose tris(3,5-dimethylphenylcarbamate) as chiral stationary phase. Chankvetadze L, Kartozia I, Yamamoto C, Chankvetadze B, Blaschke G, Okamoto Y. Electrophoresis; 2002 Feb 29; 23(3):486-93. PubMed ID: 11870751 [Abstract] [Full Text] [Related]
19. The chiral resolution of pesticides on amylose-tris(3,5-dimethylphenylcarbamate) CSP by HPLC and the enantiomeric identification by circular dichroism. Wang P, Liu D, Jiang S, Xu Y, Gu X, Zhou Z. Chirality; 2008 Jan 29; 20(1):40-6. PubMed ID: 17957825 [Abstract] [Full Text] [Related]
20. Fast enantioseparations of basic analytes by high-performance liquid chromatography using cellulose tris(3,5-dimethylphenylcarbamate)-coated zirconia stationary phases. Castells CB, Carr PW. J Chromatogr A; 2000 Dec 22; 904(1):17-33. PubMed ID: 11209898 [Abstract] [Full Text] [Related] Page: [Next] [New Search]