These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

232 related items for PubMed ID: 27834832

  • 1. 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]

  • 2. 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]

  • 3. [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 01; 29(11):1087-92. PubMed ID: 22393696
    [Abstract] [Full Text] [Related]

  • 4. Synthesis of cellulose carbamates bearing regioselective substituents at 2,3- and 6-positions for efficient chromatographic enantioseparation.
    Shen J, Wang F, Bi W, Liu B, Liu S, Okamoto Y.
    J Chromatogr A; 2018 Oct 19; 1572():54-61. PubMed ID: 30146373
    [Abstract] [Full Text] [Related]

  • 5. Synthesis and chiral recognition of amylose derivatives bearing regioselective phenylcarbamate substituents at 2,6- and 3-positions for high-performance liquid chromatography.
    Shen J, Li G, Yang Z, Okamoto Y.
    J Chromatogr A; 2016 Oct 07; 1467():199-205. PubMed ID: 27452988
    [Abstract] [Full Text] [Related]

  • 6. Effect of the solute molecular structure on its enantioresolution on cellulose tris(3,5-dimethylphenylcarbamate).
    Kasat RB, Wee SY, Loh JX, Wang NH, Franses EI.
    J Chromatogr B Analyt Technol Biomed Life Sci; 2008 Nov 01; 875(1):81-92. PubMed ID: 18635409
    [Abstract] [Full Text] [Related]

  • 7. 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 01; 378(5):1364-8. PubMed ID: 14735279
    [Abstract] [Full Text] [Related]

  • 8. [Study on enantioselectivity of celluloses derived by phenylcarbamate at 2,3- or 2,3,6-positions].
    Chang Y, Zhou L, Yuan L.
    Se Pu; 2007 Mar 01; 25(2):203-6. PubMed ID: 17580686
    [Abstract] [Full Text] [Related]

  • 9. Cellulose tris(3,5-dimethylphenylcarbamate)-coated zirconia as a chiral stationary phase for HPLC.
    Castells CB, Carr PW.
    Anal Chem; 1999 Aug 01; 71(15):3013-21. PubMed ID: 10450151
    [Abstract] [Full Text] [Related]

  • 10. Preparation of chiral stationary phase for HPLC based on immobilization of cellulose 3,5-dimethylphenylcarbamate derivatives on silica gel.
    Kubota T, Yamamoto C, Okamoto Y.
    Chirality; 2003 Jan 01; 15(1):77-82. PubMed ID: 12467047
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. Preparation of cellulose derivative bearing bulky 4-(2-benzothienyl)phenylcarbamate substituents as chiral stationary phase for enantioseparation.
    Wang F, Wang Y, Min Y, Li J, Zhang L, Zheng T, Shen J, Okamoto Y.
    Chirality; 2022 May 29; 34(5):701-710. PubMed ID: 35174536
    [Abstract] [Full Text] [Related]

  • 13. 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 29; 28(5):376-81. PubMed ID: 26949227
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. [Direct optical resolution of acidic biphenyl drugs by high performance liquid chromatography on tris(3,5-dimethylphenylcarbamate) of cellulose].
    Liu YQ, Cai QS, Yu ZW, Chang JB, Jiang SX, Chen LR.
    Se Pu; 2000 Jul 29; 18(4):287-90. PubMed ID: 12541499
    [Abstract] [Full Text] [Related]

  • 16. The preparation of a new 3,5-dichlorophenylcarbamated cellulose-bonded stationary phase and its application for the enantioseparation and determination of chiral fungicides by LC-MS/MS.
    Li L, Wang H, Shuang Y, Li L.
    Talanta; 2019 Sep 01; 202():494-506. PubMed ID: 31171212
    [Abstract] [Full Text] [Related]

  • 17. 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 01; 35(1):29-39. PubMed ID: 36323631
    [Abstract] [Full Text] [Related]

  • 18. 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]

  • 19. Exploring solvent versatility in immobilized cellulose-based chiral stationary phase for the enantioselective liquid chromatographic resolution of racemates.
    Ghanem A.
    J Sep Sci; 2007 May 26; 30(7):1019-28. PubMed ID: 17566336
    [Abstract] [Full Text] [Related]

  • 20. Cellulose tris-(3,5-dimethylphenylcarbamate)-based chiral stationary phase for the enantioseparation of drugs in supercritical fluid chromatography: comparison with HPLC.
    Kalíková K, Martínková M, Schmid MG, Tesařová E.
    J Sep Sci; 2018 Mar 26; 41(6):1471-1478. PubMed ID: 29293289
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 12.