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Russian Chemical Reviews, 1968, Volume 37, Issue 7, Pages 565–575
DOI: https://doi.org/10.1070/RC1968v037n07ABEH001668
(Mi rcr2190)
 

This article is cited in 41 scientific papers (total in 41 papers)

Chromatographic Resolution of Racemates on Dissymmetric Sorbents

S. V. Rogozhin, V. A. Davankov

A. N. Nesmeyanov Institute of Organoelement Compounds, USSR Academy of Sciences, Moscow
Abstract: The review discusses the use of natural sorbents (proteins, carbohydrates, and optically active quartz) and also artificial dissymmetric sorbents (based on silica gel and activated carbon) for the chromatography of racemates. Gas chromatography is very effective for the separation of diastereomers, but is less suitable for the direct separation of optical isomers. On the other hand, dissymmetric ion-exchange sorbents, which are considered in detail in the review, may find wider practical application. The list of references contains 197 items.
Document Type: Article
UDC: 547.466:543.54
Language: English
Original paper language: Russian


Citation: S. V. Rogozhin, V. A. Davankov, “Chromatographic Resolution of Racemates on Dissymmetric Sorbents”, Usp. Khim., 37:7 (1968), 1327–1347; Russian Chem. Reviews, 37:7 (1968), 565–575
Linking options:
  • https://www.mathnet.ru/eng/rcr2190
  • https://doi.org/10.1070/RC1968v037n07ABEH001668
  • https://www.mathnet.ru/eng/rcr/v37/i7/p1327
  • This publication is cited in the following 41 articles:
    1. Jürgen Martens, Ravi Bhushan, Separation & Purification Reviews, 53:2 (2024), 138  crossref
    2. Yuan Li, Xiao-Ning Jin, Yue Cheng, Xiao-Fei Ma, Yong Wang, J. Anal. Test., 6:2 (2022), 129  crossref
    3. Yashin Ya.I., Yashin A.Ya., J. Anal. Chem., 75:10 (2020), 1252–1263  crossref  isi
    4. David Speybrouck, Michael Howsam, Emmanuelle Lipka, TrAC Trends in Analytical Chemistry, 133 (2020), 116090  crossref
    5. Federica Ianni, Lucia Pucciarini, Andrea Carotti, Roccaldo Sardella, Benedetto Natalini, Methods in Molecular Biology, 1985, Chiral Separations, 2019, 279  crossref
    6. Federica Ianni, Lucia Pucciarini, Andrea Carotti, Serena Natalini, Gulnara Z. Raskildina, Roccaldo Sardella, Benedetto Natalini, J of Separation Science, 42:1 (2019), 21  crossref
    7. Yury A. Zolotov, Russian Contributions to Analytical Chemistry, 2018, 47  crossref
    8. V. P. Chizhkov, V. N. Boitsov, Russ. J. Phys. Chem., 91:3 (2017), 586  crossref
    9. David Sýkora, Jiří Vozka, Eva Tesařová, Květa Kalíková, Martin Havlík, Pavel Matějka, Vladimír Král, Electrophoresis, 38:15 (2017), 1956  crossref
    10. I. G. Smirnova, G. N. Gil'deeva, V. G. Kukes, Moscow Univ. Chem. Bull., 67:3 (2012), 95  crossref
    11. Ren-Qi Wang, Teng-Teng Ong, Siu-Choon Ng, Journal of Chromatography A, 1224 (2012), 97  crossref
    12. Karol Kacprzak, Jacek Gawronski, Cinchona Alkaloids in Synthesis and Catalysis, 2009, 419  crossref
    13. A. I. Vorob'eva, D. R. Sagitova, S. V. Kolesov, L. V. Spirikhin, Yu. B. Monakov, Russ J Appl Chem, 81:2 (2008), 290  crossref
    14. Aidan X. Smyth, Malcolm R. Smyth, Analytical Letters, 29:6 (1996), 991  crossref
    15. J. Martens, R. Bhushan, Journal of Liquid Chromatography, 15:1 (1992), 1  crossref
    16. Piero Salvadori, Dario Pini, Carlo Rosini, Carlo Bertucci, Gloria Uccello‐Barretta, Chirality, 4:1 (1992), 43  crossref
    17. Curt Pettersson, TrAC Trends in Analytical Chemistry, 7:6 (1988), 209  crossref
    18. William H. Pirkle, Bruce C. Hamper, Journal of Chromatography Library, 38, 1987, 235  crossref
    19. Piero Salvadori, Carlo Rosini, Dario Pini, Carlo Bertucci, Paolo Altemura, Gloria Uccello-Barretta, Andrea Raffaelli, Tetrahedron, 43:21 (1987), 4969  crossref
    20. T. Shibata, I. Okamoto, K. Ishii, Journal of Liquid Chromatography, 9:2-3 (1986), 313  crossref
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