Zobrazeno 1 - 10
of 143
pro vyhledávání: '"Gelii V. Ponomarev"'
Autor:
Evgeny S. Belyaev, Grigory L. Kozhemyakin, Vladimir S. Tyurin, Victoria V. Frolova, Ivan S. Lonin, Gelii V. Ponomarev, Aleksey K. Buryak, Ilya A. Zamilatskov
Publikováno v:
Organic & Biomolecular Chemistry. 20:1926-1932
A method of direct borylation of vinyl-substituted porphyrinoids (porphyrins and chlorins) has been developed based on the copper catalyzed vinylic C–H activation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93f46ae8c4562635aba4cc93b6644b4c
https://doi.org/10.1039/d1ob02005f
https://doi.org/10.1039/d1ob02005f
Autor:
Vladimir Zolottsev, Andrei M. Korolchuk, Artyom S. Lukin, Galina Morozevich, Arif R. Mekhtiev, Roman. A. Novikov, Yaroslav V. Tkachev, Nikita V. Suvorov, Alexander Y. Misharin, Gelii V. Ponomarev
Five new bifunctional conjugates of pyropheophorbide a with 17-substituted testosterone, dihydrotestosterone and epitestosterone differing in the length of linker (1–5) and two new complex conjugates 6 and 7 (containing three functional units: pyro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6b899beb7a26c1a1bb323950f28cbcbc
https://doi.org/10.21203/rs.3.rs-1477279/v1
https://doi.org/10.21203/rs.3.rs-1477279/v1
Autor:
Alexey A. Chistov, Alena O. Shkirdova, Vladimir S. Tyurin, Andrey V. Aralov, Ekaterina S. Kirinova, Gelii V. Ponomarev, Evgeny S. Belyaev, Ilya A. Zamilatskov, Victor A. Tafeenko, Grigory L. Kozhemyakin
Publikováno v:
Organicbiomolecular chemistry. 19(42)
Here, we investigated methods for carbene functionalization of porphyrinoids through metal catalyst-free thermal decomposition of their tosylhydrazones. For the first time, tetrapyrrolyl substituted carbenes were obtained via thermolysis of tosylhydr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d893eba7bb26daf579c4235a4699dc5a
https://pubmed.ncbi.nlm.nih.gov/34633024
https://pubmed.ncbi.nlm.nih.gov/34633024
Autor:
Dina R. Erzina, Nadezhda M. Stanetskaya, Gelii V. Ponomarev, Vladimir S. Tyurin, Vladimir V. Chernyshev, Andrew N. Fitch, Ilya A. Zamilatskov, Grigory L. Kozhemyakin
Publikováno v:
European Journal of Organic Chemistry. 2019:1508-1522
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c745b041d6fd76b1f3628c88608691d0
https://doi.org/10.1002/ejoc.201801659
https://doi.org/10.1002/ejoc.201801659
Autor:
Dmitri B. Papkovsky, Dmitri V. Yashunsky, Gelii V. Ponomarev, Alexander V. Zhdanov, Panpan Yang, Alena O. Shkirdova, Ilya A. Zamilatskov, Liang Li, Shuze Tang
Publikováno v:
Sensors and Actuators B: Chemical. 355:131116
Cell analysis by optochemical sensing represents large and important niche in life and biomedical sciences. We present advanced multi-modal, multi-analyte sensing platform and dedicated materials for cell analysis based on the substituted phosphoresc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9eb5fa3dc0f845a2038fb201f208c28
https://doi.org/10.1016/j.snb.2021.131116
https://doi.org/10.1016/j.snb.2021.131116
Autor:
Maria O. Taratynova, Gelii V. Ponomarev, Maria G. Zavialova, Yaroslav V. Tkachev, Olga V. Zazulina, Alexander Yu. Misharin, Vladimir A. Zolottsev, Vladimir P. Timofeev, Pavel N. Solyev, Galina E. Morozevich, Roman A. Novikov
Publikováno v:
Steroids. 138:82-90
Conjugates of 17α-substituted testosterone (1 and 2) and 17β-substituted epitestosterone (3 and 4) with pyropheophorbide a were synthesized. The scheme consisted of synthesis of 17α-hydroxy-3-oxopregn-4-en-21-oic and 17β-hydroxy-3-oxopregn-4-en-2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31d32ff2ab8bcd0ff718f02e8314eb78
https://doi.org/10.1016/j.steroids.2018.06.011
https://doi.org/10.1016/j.steroids.2018.06.011
Autor:
Oskar I. Koifman, Yaroslav V. Tkachev, Roman A. Novikov, Maria G. Zavialova, Gelii V. Ponomarev, Vladimir A. Zolottsev, Yulia V. Romanenko, Vladimir P. Timofeev, Maria O. Taratynova, Galina E. Morozevich, Alexander Yu. Misharin
Publikováno v:
Macroheterocycles. 11:277-285
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::088dafb35aa9715acbc301860e9a57eb
https://doi.org/10.6060/mhc180999p
https://doi.org/10.6060/mhc180999p
Autor:
Victor A. Tafeenko, V. V. Emets, Alexey A. Kostyukov, Alena O. Shkirdova, Vladimir S. Tyurin, Alexandra S. Radchenko, Vladimir A. Kuzmin, Grigory L. Kozhemyakin, Dmitry A. Cheshkov, Vitali A. Grinberg, Gelii V. Ponomarev, Evgeny S. Belyaev, Ilya A. Zamilatskov, Anton E. Egorov
Publikováno v:
Dyes and Pigments. 191:109354
A new approach to functionalize porphyrinoids was developed based on the Vilsmeier formylation followed by the azine formation and a new class of the compounds namely azines of porphyrinoids was obtained. Variously substituted azine porphyrins, chlor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1157c6ad8cd31c825f40a916747abe82
https://doi.org/10.1016/j.dyepig.2021.109354
https://doi.org/10.1016/j.dyepig.2021.109354
Autor:
Sergey A. Zverev, Gelii V. Ponomarev, Dina R. Erzina, Sergey V. Andreev, Nadezhda M. Kurochkina, Ilya A. Zamilatskov, I. N. Senchikhin, Vladimir V. Chernyshev, Vladimir S. Tyurin
Publikováno v:
Russian Journal of Physical Chemistry A. 91:1462-1467
The reaction between coproporphyrin I tetraethyl ester and ruthenium(II) dodecacarbonyl in toluene is investigated. The formation of two different products, complexes 2 and 3 of ruthenium(II) with coproporphyrin I tetraethyl ester, studied by means o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7eb19194056a084e3b2d0fa28580ed56
https://doi.org/10.1134/s0036024417080386
https://doi.org/10.1134/s0036024417080386
Autor:
Ilya A. Zamilatskov, Gelii V. Ponomarev, Dina R. Erzina, Victor A. Tafeenko, Nadezhda M. Kurochkina
Publikováno v:
Acta Crystallographica Section C Structural Chemistry. 73:68-71
The features of porphyrins defining their functionality are related to their conformational flexibility. The degree of nonplanarity of metalloporphyrins depends directly on the number of substituents, their size and their location. The introduction o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f54d2870f8502fbbbbd1e67d150d2f43
https://doi.org/10.1107/s2053229616020465
https://doi.org/10.1107/s2053229616020465