Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Olga S. Zhukova"'
Autor:
Barbara Z. Eletskaya, Maria Ya. Berzina, Ilya V. Fateev, Alexei L. Kayushin, Elena V. Dorofeeva, Olga I. Lutonina, Ekaterina A. Zorina, Konstantin V. Antonov, Alexander S. Paramonov, Inessa S. Muzyka, Olga S. Zhukova, Mikhail V. Kiselevskiy, Anatoly I. Miroshnikov, Roman S. Esipov, Irina D. Konstantinova
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 7, p 6223 (2023)
A number of purine arabinosides containing chiral amino acid amides at the C6 position of the purine were synthesized using a transglycosylation reaction with recombinant E. coli nucleoside phosphorylases. Arsenolysis of 2-chloropurine ribosides with
Externí odkaz:
https://doaj.org/article/f29fcfdbffac4cb9834047e3156d7761
Autor:
Tatiana Kulakovskaya, Nikolay E. Nifantiev, E. V. Kulakovskaya, Olga S. Zhukova, Mikhail Kiselevskiy, D. V. Yashunsky
Publikováno v:
Journal of Carbohydrate Chemistry. 34:460-474
GRAPHICAL ABSTRACTAn efficient procedure for the synthesis of cyanogenic glycosides with different carbohydrate units was developed. Amygdalin (3), prunasin (1), sambunigrin (2), and neoamygdalin (21) were prepared according to the elaborated method,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f71796705bfa51dd22bde8fe957c7c79
https://doi.org/10.1080/07328303.2015.1105249
https://doi.org/10.1080/07328303.2015.1105249
Autor:
Rujena B. Pugacheva, Nadejda P. Yavorskaya, Irina S. Golubeva, G. N. Apryshko, Vladimir Poroikov, Olga S. Zhukova, Oxana B. Kazakova, Gulnara V. Giniyatyllina, I. E. Smirnova
Publikováno v:
Medicinal Chemistry Research. 24:3423-3436
Triterpenoids with aminopropoxy groups in C-28 or C-3 and C-28 positions were synthesized from betulin, erythrodiol, uvaol, oleantriol and betulinic acid N-methylpiperazinylamide by cyanoethylation and the following catalytic hydrogenolysis. Computat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc4f456acb80f34fc2a44344364fc5f5
https://doi.org/10.1007/s00044-015-1392-y
https://doi.org/10.1007/s00044-015-1392-y