Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Cyril S. Alexeev"'
Autor:
Maria A. Konkina, Mikhail S. Drenichev, Darina I. Nasyrova, Yuri B. Porozov, Cyril S. Alexeev
Publikováno v:
Sustainable Chemistry and Pharmacy. 32:101011
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6038b37d945ae07b22465e3489546a0c
https://doi.org/10.1016/j.scp.2023.101011
https://doi.org/10.1016/j.scp.2023.101011
Autor:
Mikhail S, Drenichev, Vladimir E, Oslovsky, Anastasia A, Zenchenko, Claudia V, Danilova, Mikhail A, Varga, Roman S, Esipov, Dmitry D, Lykoshin, Cyril S, Alexeev
Publikováno v:
International journal of molecular sciences. 23(5)
A comparative analysis of the transglycosylation conditions catalyzed by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::816407cbe5c0f4f5daa6b9ffc1d203e7
https://pubmed.ncbi.nlm.nih.gov/35269937
https://pubmed.ncbi.nlm.nih.gov/35269937
Autor:
Mikhail S. Drenichev, Vladimir E. Oslovsky, Anastasia A. Zenchenko, Claudia V. Danilova, Mikhail A. Varga, Roman S. Esipov, Dmitry D. Lykoshin, Cyril S. Alexeev
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 5; Pages: 2795
A comparative analysis of the transglycosylation conditions catalyzed by E. coli nucleoside phosphorylases, leading to the formation of 2′-deoxynucleosides, was performed. We demonstrated that maximal yields of 2′-deoxynucleosides, especially mod
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b055d6e1219c85ca7f6ab94a5f8a45c
https://doi.org/10.3390/ijms23052795
https://doi.org/10.3390/ijms23052795
Autor:
Cyril S. Alexeev, Irina V. Kulikova, Vitali I. Tararov, Sergei Gavryushov, Sergey N. Mikhailov
Publikováno v:
Advanced Synthesis & Catalysis. 360:3090-3096
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5678b96fbdf7e4b69960c4ed914f86e
https://doi.org/10.1002/adsc.201800411
https://doi.org/10.1002/adsc.201800411
Publikováno v:
Advanced Synthesis & Catalysis. 360:305-312
Enzymatic transglycosylation - a transfer of the carbohydrate moiety from one heterocyclic base to another - is being actively developed and applied for the synthesis of practically important nucleosides. This reaction is catalyzed by nucleoside phos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::411ea35c9a9ab2aaf85d5bf9f3573197
https://doi.org/10.1002/adsc.201701005
https://doi.org/10.1002/adsc.201701005
Autor:
Sergey N. Mikhailov, Roman S. Esipov, Cyril S. Alexeev, Irina V. Kulikova, Mikhail S. Drenichev, Evgeniya O. Dorinova
Publikováno v:
Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics. 1868:140292
Enzymatic transglycosylation, a transfer of the carbohydrate moiety from one heterocyclic base to another, is catalyzed by nucleoside phosphorylases (NPs) and is being actively developed and applied for the synthesis of biologically important nucleos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81f460925f37854604bcafa90271b19e
https://doi.org/10.1016/j.bbapap.2019.140292
https://doi.org/10.1016/j.bbapap.2019.140292
Autor:
Pavel N. Solyev, Cyril S. Alexeev, Sergey N. Mikhailov, Mikhail S. Drenichev, Vladimir E. Oslovsky, Roman S. Esipov
Publikováno v:
Current protocols in nucleic acid chemistry. 75(1)
This unit describes an effective method for the preparation of natural cytokinins and their synthetic derivatives based on enzymatic cleavage of the N-glycosidic bond of N6 -substituted adenosine or O6 -substituted inosine derivatives in the presence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::038ed0c599c61b9eb8cccee21e6b7d15
https://pubmed.ncbi.nlm.nih.gov/30299587
https://pubmed.ncbi.nlm.nih.gov/30299587
Publikováno v:
Synthesis. 2011:2483-2489
A simple and efficient route to N 6 -acetyl-2′,3′,5′-tri- O-acetyladenosine ( 1)was developed based on selective N-deacetylation of pentaacetylatedadenosine 2 with methanol at room temperaturein the presence of imidazole. Preparative synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1bfa614fa4a2a3e1dcc0645d647dc0cc
https://doi.org/10.1055/s-0030-1260090
https://doi.org/10.1055/s-0030-1260090
Autor:
Eliso Solomko, Svetlana V. Kolyachkina, Georgy A. Romanov, Evgenia V. Stepanova, Sergey N. Mikhailov, Dmitry M. Krivosheev, Andrey N. Inshakov, Vitali I. Tararov, Cyril S. Alexeev
Publikováno v:
Collection of Czechoslovak Chemical Communications. 76:1361-1378
A series of N6-adenosine derivatives were synthesized by alkylation of N6-acetyl-2′,3′,5′-tri-O-acetyladenosine (1) with alkyl halides and alcohols. It was shown that propargyl derivative 2a is a good substrate for copper(I) catalyzed Huisgen [
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e792c5b2284bb808c12d0abd6a1f7ca4
https://doi.org/10.1135/cccc2011114
https://doi.org/10.1135/cccc2011114
Publikováno v:
Collection Symposium Series.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cbfedd1647e59748cbe6f2a8e63c88f6
https://doi.org/10.1135/css201414213
https://doi.org/10.1135/css201414213