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V A Khripach

Showing results (1-10 of 24) with videos related to

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Bioorganicheskaia Khimiia|June 25, 2002
[Novel synthesis of zymosterol]A V Baranovskiĭ, R P Litvinovskaia, V A Khripach
Bioorganicheskaia Khimiia|August 13, 2008
[Synthesis of sterols oxygenated in the terminal fragment of their side chains]A V Antonchik, V N Zhabinskiĭ, V A Khripach
Bioorganicheskaia Khimiia|August 9, 2007
[Oxysterols: genesis and basic functions]A V Antonchik, V N Zhabinskiĭ, V A Khripach
Organic & Biomolecular Chemistry|November 13, 2014
Formation of the steroidal C-25 chiral center via the asymmetric alkylation methodologyYu V Ermolovich, V N Zhabinskii, V A Khripach
Bioorganicheskaia Khimiia|May 5, 2007
[A new synthesis of cerebrosterol and its 24-epimer from lithocholic acid]V A Khripach, V N Zhabinskiĭ, A V Antonchik
Organic & Biomolecular Chemistry|December 5, 2014
The development and use of a general route to brassinolide, its biosynthetic precursors, metabolites and analoguesA L Hurski, Yu V Ermolovich, V N Zhabinskii, et al.
Bioorganicheskaia Khimiia|August 9, 2007
[The synthesis of 2alpha,3alpha-isopropylidenedioxy-6,6-ethylenedioxy-5alpha-androst-15-en-17-one and its 2beta,3beta-isomer]R P Litvinovskaia, A V Baranovskiĭ, M A Aver'kova, et al.
Bioorganicheskaia Khimiia|December 22, 2006
[Synthesis of (24S)-hydroxy- and (24S)-24,25-epoxycholesterol analogues, potential agonists of nuclear LXR receptors]V A Khripach, V N Zhabinskiĭ, A V Antonchik, et al.
Doklady. Biochemistry and Biophysics|March 11, 2022
Comparison of Protective Reactions of Rape Seeds to Chloride Salination at Exposure to Epibrassinolide before or during Salt StressL V Kolomeichuk, V A Khripach, V V Kuznetsov, et al.
Bioorganicheskaia Khimiia|June 20, 2009
[Synthesis of brassinolide and its biosynthetic precursors using methyl-3-hydroxy-2-methylpropionate]V A Khripach, V N Zhabinskiĭ, K V Parkhimovich, et al.
Pageof 3

Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Bioorganicheskaia Khimiia|June 25, 2002
[Novel synthesis of zymosterol]A V Baranovskiĭ, R P Litvinovskaia, V A Khripach
Bioorganicheskaia Khimiia|August 13, 2008
[Synthesis of sterols oxygenated in the terminal fragment of their side chains]A V Antonchik, V N Zhabinskiĭ, V A Khripach
Bioorganicheskaia Khimiia|August 9, 2007
[Oxysterols: genesis and basic functions]A V Antonchik, V N Zhabinskiĭ, V A Khripach
Organic & Biomolecular Chemistry|November 13, 2014
Formation of the steroidal C-25 chiral center via the asymmetric alkylation methodologyYu V Ermolovich, V N Zhabinskii, V A Khripach
Bioorganicheskaia Khimiia|May 5, 2007
[A new synthesis of cerebrosterol and its 24-epimer from lithocholic acid]V A Khripach, V N Zhabinskiĭ, A V Antonchik
Organic & Biomolecular Chemistry|December 5, 2014
The development and use of a general route to brassinolide, its biosynthetic precursors, metabolites and analoguesA L Hurski, Yu V Ermolovich, V N Zhabinskii, et al.
Bioorganicheskaia Khimiia|August 9, 2007
[The synthesis of 2alpha,3alpha-isopropylidenedioxy-6,6-ethylenedioxy-5alpha-androst-15-en-17-one and its 2beta,3beta-isomer]R P Litvinovskaia, A V Baranovskiĭ, M A Aver'kova, et al.
Bioorganicheskaia Khimiia|December 22, 2006
[Synthesis of (24S)-hydroxy- and (24S)-24,25-epoxycholesterol analogues, potential agonists of nuclear LXR receptors]V A Khripach, V N Zhabinskiĭ, A V Antonchik, et al.
Doklady. Biochemistry and Biophysics|March 11, 2022
Comparison of Protective Reactions of Rape Seeds to Chloride Salination at Exposure to Epibrassinolide before or during Salt StressL V Kolomeichuk, V A Khripach, V V Kuznetsov, et al.
Bioorganicheskaia Khimiia|June 20, 2009
[Synthesis of brassinolide and its biosynthetic precursors using methyl-3-hydroxy-2-methylpropionate]V A Khripach, V N Zhabinskiĭ, K V Parkhimovich, et al.
Pageof 3