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Journal Abstract Search

230 related items for PubMed ID: 35635867

  • 1. 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
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  • 4. Enantioseparation characteristics of biselector chiral stationary phases based on derivatives of cellulose and amylose.
    Wang ZQ, Liu JD, Chen W, Bai ZW.
    J Chromatogr A; 2014 Jun 13; 1346():57-68. PubMed ID: 24792697
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  • 5. [Preparation and evaluation of amylose and cellulose tris (3-trifluoromethylphenylcarbamates)-based chiral stationary phases].
    Jin Z, Hu F, Wang Y, Liu G, Wang F, Pan F, Tang S.
    Se Pu; 2011 Nov 13; 29(11):1087-92. PubMed ID: 22393696
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  • 7. Graphene quantum dots functionalized β-cyclodextrin and cellulose chiral stationary phases with enhanced enantioseparation performance.
    Wu Q, Gao J, Chen L, Dong S, Li H, Qiu H, Zhao L.
    J Chromatogr A; 2019 Aug 30; 1600():209-218. PubMed ID: 31047665
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  • 8. Enantioseparation and molecular modeling study of chiral amines as three naphthaldimine derivatives using amylose or cellulose trisphenylcarbamate chiral stationary phases.
    Adhikari S, Bhujbal S, Paik MJ, Lee W.
    Chirality; 2023 Jan 30; 35(1):29-39. PubMed ID: 36323631
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  • 9. 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
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  • 10. Construction of a hydrazone-linked chiral covalent organic framework-silica composite as the stationary phase for high performance liquid chromatography.
    Zhang K, Cai SL, Yan YL, He ZH, Lin HM, Huang XL, Zheng SR, Fan J, Zhang WG.
    J Chromatogr A; 2017 Oct 13; 1519():100-109. PubMed ID: 28899554
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  • 11. Liquid chromatographic enantiomer separation of 1-naphthylamides of chiral acids using several amylose- and cellulose-derived chiral stationary phases.
    Islam MF, Adhikari S, Paik MJ, Lee W.
    Arch Pharm Res; 2017 Mar 13; 40(3):350-355. PubMed ID: 28074398
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  • 12. Synthesis and characterization of cellulose 3,5-dimethylphenylcarbamate silica hybrid spheres for enantioseparation of chiral β-blockers.
    Weng X, Bao Z, Xing H, Zhang Z, Yang Q, Su B, Yang Y, Ren Q.
    J Chromatogr A; 2013 Dec 20; 1321():38-47. PubMed ID: 24231262
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  • 13. Preparation and evaluation of regioselectively substituted amylose derivatives for chiral separations.
    Tang S, Jin Z, Sun B, Wang F, Tang W.
    Chirality; 2017 Sep 20; 29(9):512-521. PubMed ID: 28635058
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  • 14. Synthesis of substituted phenylcarbamates of N-cyclobutylformylated chitosan and their application as chiral selectors in enantioseparation.
    Zhang J, Wang XC, Chen W, Bai ZW.
    Analyst; 2016 Jul 04; 141(14):4470-80. PubMed ID: 27191623
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  • 16. Comparison of several polysaccharide-derived chiral stationary phases for the enantiomer separation of N-fluorenylmethoxycarbonyl alpha-amino acids by HPLC.
    Jin JY, Lee KA, Kang JS, Kang YK, Baek CS, Lee W.
    Arch Pharm Res; 2007 May 04; 30(5):659-64. PubMed ID: 17615688
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  • 17. Construction of dual-chiral covalent organic frameworks for enantioselective separation.
    Ma J, Huang W, Huang X, Yang N, Gong J, Xie Z, Li G, Liao Q, Chen Y.
    J Chromatogr A; 2024 Aug 02; 1728():465014. PubMed ID: 38797135
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  • 20. Engineering thiol-ene click chemistry for the preparation of a chiral stationary phase based on a [4+6]-type homochiral porous organic cage for enantiomeric separation in normal-phase and reversed-phase high performance liquid chromatography.
    Liang RX, Zhang YP, Zhang JH, Gong YN, Huang B, Wang BJ, Xie SM, Yuan LM.
    J Chromatogr A; 2023 Nov 22; 1711():464444. PubMed ID: 37837712
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