Zobrazeno 1 - 10
of 99
pro vyhledávání: '"A. L. Rodina"'
Autor:
Liudmila L. Rodina, Xenia V. Azarova, Jury J. Medvedev, Dmitrij V. Semenok, Valerij A. Nikolaev
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 2250-2258 (2018)
The sensitized photoexcitation of 2-diazocyclopentane-1,3-diones in the presence of THF leads to the insertion of the terminal N-atom of the diazo group into the α-С–Н bond of THF, producing the associated N-alkylhydrazones in yields of up to 63
Externí odkaz:
https://doaj.org/article/676c9dc824c94b58807eadbc3db09d14
Autor:
E. D. Verbovaya, A. L. Rodina
Publikováno v:
Medical alphabet. :103-106
The article deals epidemiology, pathomorphological picture, trigger factors of development, peculiarities of treatment with the use of botulinum therapy for rosacea. A clinical case is presented.Purpose of the article. Consider the pathogenesis of ro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::241dcd2ea566eea730289bbf08469a49
https://doi.org/10.33667/2078-5631-2022-8-103-106
https://doi.org/10.33667/2078-5631-2022-8-103-106
Autor:
Andrey S. Mereshchenko, Alexey V. Ivanov, Viktor I. Baranovskii, Grzegorz Mloston, Ludmila L. Rodina, Valerij A. Nikolaev
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 504-513 (2015)
The 1,3-dipolar cycloaddition of acyclic 2-diazo-1,3-dicarbonyl compounds (DDC) and thioketones preferably occurs with Z,E-conformers and leads to the formation of transient thiocarbonyl ylides in two stages. The thermodynamically favorable further t
Externí odkaz:
https://doaj.org/article/fbb88b3c0612491c8327977cc4d593f6
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 2751-2761 (2013)
Acyclic diazodicarbonyl compounds react at room temperature with cycloaliphatic thioketones, e.g. 2,2,4,4-tetramethyl-3-thioxocyclobutanе-1-one and adamantanethione, via a cascade process in which the key step is a 1,5-electrocyclization of the inte
Externí odkaz:
https://doaj.org/article/366eec6f6d684329b13ea0f2fc30e006
Autor:
Dmitrij V Semenok, Jury J. Medvedev, Valerij A. Nikolaev, Liudmila L. Rodina, Xenia V. Azarova
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 2250-2258 (2018)
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 2250-2258 (2018)
The sensitized photoexcitation of 2-diazocyclopentane-1,3-diones in the presence of THF leads to the insertion of the terminal N-atom of the diazo group into the α-С–Н bond of THF, producing the associated N-alkylhydrazones in yields of up to 63
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9968a066627c1cf1fc3ca3a44a727370
https://doi.org/10.3762/bjoc.14.200
https://doi.org/10.3762/bjoc.14.200
Autor:
M. S. Novikov, K. I. Kobrakov, Alexander S. Semeikin, Yu. N. Klimochkin, Fedor I. Zubkov, S. M. Medvedeva, Elena L. Gavrilova, L. G. Voskresenskii, Valery N. Charushin, Albert T. Lebedev, Alexander V. Aksenov, Ludmila L. Rodina, S. V. Kurbatov, Sergey M. Ivanov, Alexander P. Molchanov, Irina P. Beletskaya, Oleg N. Chupakhin, Elena A. Krasnokutskaya, Nicolai A. Aksenov, L. M. Mironovich, D. N. Kuznetsov, L. Ya. Zakharova, Mikhail P. Koroteev, Vad. V. Negrebetskii, O. A. Golubchikov, A. S. Fisyuk, A. V. Kolobov, Sergey Z. Vatsadze, Sergey P. Gromov, Vitaly A. Osyanin, Igor S. Antipin, Ivan I. Stoikov, A. I. Konovalov, Almira Kurbangalieva, Mikhail A. Kuznetsov, E. R. Kofanov, Victor D. Filimonov, Pavel A. Stuzhin, Valerij A. Nikolaev, A. Yu. Egorova, Nikolai V. Zyk, Alexander F. Khlebnikov, M. K. Grachev, Vladimir Burilov, Kh. S. Shikhaliev, Igor G. Zenkevich, Timur I. Madzhidov, Alexander N. Reznikov, D. B. Berezin, Svetlana E. Solovieva, Dmitrii A. Lemenovskii, Yu. I. Baukov, Valerii F. Traven, Andrey E. Shchekotikhin, A. Yu. Fedorov, R. S. Begunov, A. I. Rusakov, Valery S. Petrosyan, Alexander S. Tikhomirov, O. N. Burov, Mikhail S. Tovbis, T. A. Shmigol, O. V. Fedotova, V. Yu. Orlov, G. A. Suboch, A. K. Brel, V. I. Maslennikova, G. P. Sagitullina, M. Yu. Krasavin, Vakhid A. Mamedov, A. V. Nemtarev, S. V. Lisina, Aleksander V. Vasilyev, Alexander A. Korlyukov, V. G. Nenaidenko, M. E. Kletskii, Irina A. Balova, Oleg G. Sinyashin, Alexander V. Nyuchev
Publikováno v:
Russian Journal of Organic Chemistry. 54:157-371
This review is devoted to the scientific achievements of the departments of organic chemistry in higher schools of Russia within the past decade.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a2610e72d45c2bf6f33b0cc80643075
https://doi.org/10.1134/s107042801802001x
https://doi.org/10.1134/s107042801802001x
Autor:
Michael E. Weinblatt, Asta Baranauskaite, Jaroslaw Niebrzydowski, Eva Dokoupilova, Agnieszka Zielinska, Janusz Jaworski, Artur Racewicz, Margarita Pileckyte, Krystyna Jedrychowicz‐Rosiak, Soo Yeon Cheong, Jeehoon Ghil, S. Sokolovic, M. Mekic, N. Prodanovic, B. Gajic, E. Karaselimovic‐Dzambasovic, B. Pojskic, A. Toncheva, P. Dimitar, L. Rodina, M. Geneva‐Popova, I. Staykov, R. Stoilov, L. Podrazilova, Z. Mosterova, G. Simkova, J. Kopackova, Z. Stejfova, J. Vencovsky, Z. Urbanova, L. Janska, D. Galatíkova, S. Stropuviene, I. Sniuoliene, K. Sitek‐Ziolkowska, M. Rell‐Bakalarska, R. Kolasa, S. Daniluk, B. Sliwowska, M. Bartosik‐Twardowska, J. Brzezicki, M. Konieczny, S. Jeka, J. Choe, S. Bae, Y. Kang, L. Prystupa, Z. Vyacheslav, I. Gasanov, R. Yatsyshyn, D. Rekalov, O. Iaremenko, M. Stanislavchuk, V. Tseluyko
Publikováno v:
Arthritis & Rheumatology (Hoboken, N.j.)
Objective SB5 is a biosimilar agent for adalimumab (ADA). The aim of this study was to evaluate the efficacy, pharmacokinetics (PK), safety, and immunogenicity of SB5 in comparison with reference ADA in patients with rheumatoid arthritis (RA). Method
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd57157bedc7b756d3a592490108b340
https://doi.org/10.1002/art.40336
https://doi.org/10.1002/art.40336
Autor:
Liudmila L. Rodina, Nina L. Tonogina, Victor I. Baranovskii, Valerij A. Nikolaev, Alexey Povolotskiy, Olesia S. Galkina
Publikováno v:
The Journal of Organic Chemistry. 82:11399-11405
The energies and lifetimes of the excited states (S1, S2, S5, T1) of a diazotetrahydrofuranone were determined using experimental and computational methods. It was shown that direction of the diazoketone photochemical transformations without eliminat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65b613d0adabd5da4559d0941f71aa45
https://doi.org/10.1021/acs.joc.7b01848
https://doi.org/10.1021/acs.joc.7b01848
Autor:
Xenia V. Azarova, Dmitrii V. Semenok, Jury J. Medvedev, Liudmila L. Rodina, Valerij A. Nikolaev
Publikováno v:
Synthesis. 48:4525-4532
The interaction of 5,5-dialkyl(diaryl)-substituted 4-diazo-3(2H)furanones with Bronsted acids (TFA, TsOH, etc.) causes elimination of nitrogen accompanied by 1,2-nucleophilic rearrangement, giving rise to exclusive formation of 4,5-dialkyl(diaryl)-su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d5d4f509e6fc09802122409bd3a04da
https://doi.org/10.1055/s-0036-1588304
https://doi.org/10.1055/s-0036-1588304
Publikováno v:
ResearcherID
Benzophenone-sensitized reactions of 4-diazotetrahydrofuran-3(2H)-ones with H-donors such as tetrahydrofuran, 1,4-dioxane, cyclohexane and diethyl ether, occur without elimination of nitrogen and give rise to the corresponding N-substituted hydrazone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b34a7a8db52658d17edda9e620131b1
https://doi.org/10.1002/ajoc.201600050
https://doi.org/10.1002/ajoc.201600050