Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Andrey I. Taratayko"'
Autor:
Sergey A. Dobrynin, Mark M. Gulman, Denis A. Morozov, Irina F. Zhurko, Andrey I. Taratayko, Yulia S. Sotnikova, Yurii I. Glazachev, Yuri V. Gatilov, Igor A. Kirilyuk
Publikováno v:
Molecules, Vol 27, Iss 21, p 7626 (2022)
Sterically shielded nitroxides, which demonstrate high resistance to bioreduction, are the spin labels of choice for structural studies inside living cells using pulsed EPR and functional MRI and EPRI in vivo. To prepare new sterically shielded nitro
Externí odkaz:
https://doaj.org/article/6e297bd7718949f79b7020649bc3617d
Autor:
Yulia V. Khoroshunova, Denis A. Morozov, Andrey I. Taratayko, Polina D. Gladkikh, Yuri I. Glazachev, Igor A. Kirilyuk
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 2036-2042 (2019)
Sterically shielded nitroxides of the pyrrolidine series have shown the highest resistance to reduction. Here we report the synthesis of new pyrrolidine nitroxides from 5,5-dialkyl-1-pyrroline N-oxides via the introduction of a pent-4-enyl group to t
Externí odkaz:
https://doaj.org/article/5dc88386e677414789fef0c941307747
Publikováno v:
Molecules, Vol 27, Iss 6, p 1922 (2022)
Pyrrolidine nitroxides with four bulky alkyl substituents adjacent to N–O group are known for their high resistance to bioreduction. The 3,4-unsubstituted 2-tert-butyl-2-ethylpyrrolidine-1-oxyls were prepared from the corresponding 2-tert-butyl-1-p
Externí odkaz:
https://doaj.org/article/8c9cdcde5c6f4e3a8e3e5a82e01783d3
Autor:
Yulia V. Khoroshunova, Denis A. Morozov, Andrey I. Taratayko, Sergey A. Dobrynin, Ilia V. Eltsov, Tatyana V. Rybalova, Yulia S. Sotnikova, Dmitriy N. Polovyanenko, Nargiz B. Asanbaeva, Igor A. Kirilyuk
Publikováno v:
Molecules, Vol 26, Iss 19, p 6000 (2021)
Activation of a hydroxyl group towards nucleophilic substitution via reaction with methanesulfonyl chloride or PPh3-CBr4 system is a commonly used pathway to various functional derivatives. The reactions of (5R(S),6R(S))-1-X-6-(hydroxymethyl)-2,2-dim
Externí odkaz:
https://doaj.org/article/16e2e03af9cc40ca86af1d100a8219e9
Autor:
Andrey I. Taratayko, Christina S. Becker, Igor’ A. Grigor’ev, Yurii V. Gatilov, Tatyana V. Rybalova, Vladimir A. Reznikov
Publikováno v:
ARKIVOC, Vol 2013, Iss 4, Pp 272-290 (2013)
Externí odkaz:
https://doaj.org/article/42f07cf9002e440da51e039ada5ab9c3
Publikováno v:
Tetrahedron Letters. :154546
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1a6d75ea465d94a9b3303a62ef42bc0d
https://doi.org/10.1016/j.tetlet.2023.154546
https://doi.org/10.1016/j.tetlet.2023.154546
Publikováno v:
Molecules (Basel, Switzerland). 27(6)
Pyrrolidine nitroxides with four bulky alkyl substituents adjacent to N-O group are known for their high resistance to bioreduction. The 3,4-unsubstituted 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b21ad9954e1457f3a376892eecb9ceb9
https://pubmed.ncbi.nlm.nih.gov/35335285
https://pubmed.ncbi.nlm.nih.gov/35335285
Autor:
Sergey A. Dobrynin, Igor A. Kirilyuk, Denis A. Morozov, Andrey I. Taratayko, Dmitriy N. Polovyanenko, Yulia S. Sotnikova, Tatyana V. Rybalova, Yulia V. Khoroshunova, Nargiz B. Asanbaeva, Ilia V. Eltsov
Publikováno v:
Molecules, Vol 26, Iss 6000, p 6000 (2021)
Molecules
Volume 26
Issue 19
Molecules
Volume 26
Issue 19
Activation of a hydroxyl group towards nucleophilic substitution via reaction with methanesulfonyl chloride or PPh3-CBr4 system is a commonly used pathway to various functional derivatives. The reactions of (5R(S),6R(S))-1-X-6-(hydroxymethyl)-2,2-dim
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cb7e36641d4ac345c5e52d9c966e94e
https://www.mdpi.com/1420-3049/26/19/6000
https://www.mdpi.com/1420-3049/26/19/6000
Publikováno v:
The Journal of Physical Chemistry B. 123:5916-5929
The delayed radiation-induced fluorescence from polyethylene and its alkyl- and fluorine-substituted analogues doped with aromatic luminophores was studied in the time range of 1-1000 ns. Qualitative analysis of the effects of a magnetic field on the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e36ad8d24f46154d60fdca7089d12aa3
https://doi.org/10.1021/acs.jpcb.9b03914
https://doi.org/10.1021/acs.jpcb.9b03914
Autor:
Igor A. Kirilyuk, Gerd Buntkowsky, Victor M. Tormyshev, Andrey I. Taratayko, Torsten Gutmann, Vytautas Klimavicius, Dmitriy Parkhomenko, Jens Nowag, Evgenii V. Amosov, Markus M. Hoffmann, Andrey A. Kuzhelev, Elena G. Bagryanskaya, Sarah Bothe, Tatiana I. Troitskaya
Publikováno v:
The Journal of Physical Chemistry C. 122:11422-11432
Synthesis of novel trityl-nitroxyl biradicals and their performance as polarization agents in DNP-enhanced solid-state MAS NMR spectroscopy is presented. Signal enhancements in 1H, 1H → 13C CP MAS, and 13C MAS experiments obtained with these radica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e44a54fbbee33017847bb6bd74fa5824
https://doi.org/10.1021/acs.jpcc.8b02570
https://doi.org/10.1021/acs.jpcc.8b02570