Search Results - "Vatsadze, Sergey Z."

Stereoelectronic Chameleons: The Donor–Acceptor Dichotomy of Functional Groups by Vatsadze, Sergey Z., Loginova, Yulia D., dos Passos Gomes, Gabriel, Alabugin, Igor V.

“…Stereoelectronic factors account for the apparent reversal of donor–acceptor properties of a variety of functional groups by a simple change of their…”
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“Stereoelectronic Deprotection of Nitrogen”: Recovering Nucleophilicity with a Conformational Change by Gazizov, Almir S., Smolobochkin, Andrey V., Rizbayeva, Tanzilya S., Vatsadze, Sergey Z., Burilov, Alexander R., Sinyashin, Oleg G., Alabugin, Igor V.

“…Ureas are often thought of as “double amides” due to the obvious structural similarity of these functional groups. The main structural feature of an amide is…”
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Photoprocesses in Bis-Diethylamino Derivatives of 1,4- and 1,3-Distyrylbenzene by Atabekyan, Levon S, Avakyan, Vitaly G, Fomina, Marina V, Nuriev, Vyacheslav N, Medved'ko, Alexey V, Vatsadze, Sergey Z, Gromov, Sergey P, Chibisov, Alexander K

“…The photoprocesses of diethylamino derivatives of 1,4- and 1,3-distyrylbenzenes in MeCN were studied using absorption, luminescence, H NMR, and laser kinetic…”
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On the design of new europium heteroaromatic carboxylates for OLED application by Koshelev, Daniil S., Chikineva, Tatyana Yu, Kozhevnikova (Khudoleeva), Vladislava Yu, Medvedko, Alexey V., Vashchenko, Andrey A., Goloveshkin, Alexander S., Tsymbarenko, Dmitry M., Averin, Alexey A., Meschkov, Anna, Schepers, Ute, Vatsadze, Sergey Z., Utochnikova, Valentina V.

“…The approach to the directed synthesis of lanthanide aromatic carboxylates – precursors to the electroluminescent materials, - was proposed, namely the…”
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Photoprocesses in Derivatives of 1,4- and 1,3-Diazadistyryldibenzenes by Atabekyan, Levon S, Freidzon, Alexandra Y, Ionov, Dmitry S, Nuriev, Vyacheslav N, Medved'ko, Alexey V, Vatsadze, Sergey Z, Gromov, Sergey P, Chibisov, Alexander K

“…Photoprocesses in 1,4-diazadistyrylbenzene ( ) and 1,3-diazadistyrylbenzene derivative ( ) diperchlorates in MeCN were studied by absorption, luminescence, and…”
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Bispidine Platform as a Tool for Studying Amide Configuration Stability by Krut'ko, Dmitry P, Medved'ko, Alexey V, Lyssenko, Konstantin A, Churakov, Andrei V, Dalinger, Alexander I, Kalinin, Mikhail A, Gudovannyy, Alexey O, Ponomarev, Konstantin Y, Suslov, Eugeny V, Vatsadze, Sergey Z

“…In this work, the solution conformations of seventeen 3,7-diacyl bispidines were studied by means of NMR spectroscopy including VT NMR experiments. The acyl…”
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Novel Bispidine-Monoterpene Conjugates-Synthesis and Application as Ligands for the Catalytic Ethylation of Chalcones by Suslov, Evgeniy V, Ponomarev, Konstantin Y, Patrusheva, Oxana S, Kuranov, Sergey O, Okhina, Alina A, Rogachev, Artem D, Munkuev, Aldar A, Ottenbacher, Roman V, Dalinger, Alexander I, Kalinin, Mikhail A, Vatsadze, Sergey Z, Volcho, Konstantin P, Salakhutdinov, Nariman F

“…A number of new chiral bispidines containing monoterpenoid fragments have been obtained. The bispidines were studied as ligands for Ni-catalyzed addition of…”
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Bispidine-Based Macrocycles: Achievements and Perspectives by Medved’ko, Aleksei V., Gaisen, Savelii V., Kalinin, Mikhail A., Vatsadze, Sergey Z.

“…This review presents all currently known macroheterocyclic compounds that include a bispidine (3,7-diazabicyclo[3.3.1]nonane) fragment in their structure. A…”
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Reaction of β-Nitrostyrene with Diethyl Malonate in the Presence of Bispidines: The Unusual Role of the Organocatalyst by Dalinger, Alexander I., Mamedova, Sabina F., Burykina, Julia V., Pentsak, Evgeniy O., Vatsadze, Sergey Z.

“…The aim of this work was the investigation of novel organocatalysts for the Michael addition of diethyl malonate to β-nitrostyrene. The methodology of the…”
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Plier Ligands for Trapping Neurotransmitters into Complexes for Sensitive Analysis by SERS Spectroscopy by Eremina, Olga E, Kapitanova, Olesya O, Medved'ko, Alexei V, Zelenetskaya, Alexandra S, Egorova, Bayirta V, Shekhovtsova, Tatyana N, Vatsadze, Sergey Z, Veselova, Irina A

“…Catecholamines-dopamine, noradrenaline and adrenaline are important biomarkers of neurotransmitter metabolism, indicating neuroendocrine tumors and…”
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The main protease 3CLpro of the SARS-CoV-2 virus: how to turn an enemy into a helper by Belenkaya, Svetlana V, Merkuleva, Iuliia A, Yarovaya, Olga I, Chirkova, Varvara Yu, Sharlaeva, Elena A, Shanshin, Daniil V, Volosnikova, Ekaterina A, Vatsadze, Sergey Z, Khvostov, Mikhail V, Salakhutdinov, Nariman F, Shcherbakov, Dmitriy N

“…Despite the long history of use and the knowledge of the genetics and biochemistry of , problems are still possible in obtaining a soluble form of recombinant…”
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Corrigendum: The main protease 3CLpro of the SARS-CoV-2 virus: how to turn an enemy into a helper by Belenkaya, Svetlana V., Merkuleva, Iuliia A., Yarovaya, Olga I., Chirkova, Varvara Yu, Sharlaeva, Elena A., Shanshin, Daniil V., Volosnikova, Ekaterina A., Vatsadze, Sergey Z., Khvostov, Mikhail V., Salakhutdinov, Nariman F., Shcherbakov, Dmitriy

“…[This corrects the article DOI: 10.3389/fbioe.2023.1187761.]…”
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Structure–Property Relationships of Dibenzylidenecyclohexanones by Fomina, Marina V, Vatsadze, Sergey Z, Freidzon, Alexandra Ya, Kuz’mina, Lyudmila G, Moiseeva, Anna A, Starostin, Roman O, Nuriev, Vyacheslav N, Gromov, Sergey P

“…A series of symmetrical dibenzylidene derivatives of cyclohexanone were synthesized with the goal of studying the physicochemical properties of…”
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Isonitriles as Stereoelectronic Chameleons: The Donor–Acceptor Dichotomy in Radical Additions by Gomes, Gabriel dos Passos, Loginova, Yulia, Vatsadze, Sergey Z, Alabugin, Igor V

“…Radical addition to isonitriles (isocyanides) starts and continues all the way to the transition state (TS) mostly as a simple addition to a polarized π-bond…”
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Ferrocene-contained metal organic frameworks: From synthesis to applications by Huang, Zhikun, Yu, Haojie, Wang, Li, Liu, Xiaowei, Lin, Tengfei, Haq, Fazal, Vatsadze, Sergey Z., Lemenovskiy, Dmitry A.

“…•The Fc-contained MOFs was first reviewed.•The Fc-contained MOFs can be clearly divided into four basic categories.•The synthesis methods of Fc-contained MOFs…”
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Preparation of Ferrocene‐Terminated Dendrimers for the Thermal Decomposition of Ammonium Perchlorate by Liu, Jinyi, Yu, Haojie, Wang, Li, Chen, Tao, Vatsadze, Sergey Z., Chen, Dingning, Shen, Di, Wang, Yu

“…As a common oxidizer, ammonium perchlorate (AP) is an important component in composite solid propellants (CSPs). Ferrocene (Fc)‐based compounds are often…”
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Copper–Bispidine Complexes: Synthesis and Complex Stability Study by Medved’ko, Aleksei V, Egorova, Bayirta V, Komarova, Alina A, Rakhimov, Rustem D, Krut’ko, Dmitri P, Kalmykov, Stepan N, Vatsadze, Sergey Z

“…A new series of dicarboxylic derivatives of bispidines have been synthesized to develop novel copper­(II) complexes suitable as imaging agents for positron…”
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Supramolecular Organogels Based on N -Benzyl, N' -Acylbispidinols by Medved'ko, Alexey V, Dalinger, Alexander I, Nuriev, Vyacheslav N, Semashko, Vera S, Filatov, Andrei V, Ezhov, Alexander A, Churakov, Andrei V, Howard, Judith A K, Shiryaev, Andrey A, Baranchikov, Alexander E, Ivanov, Vladimir K, Vatsadze, Sergey Z

“…The acylation of unsymmetrical -benzylbispidinols in aromatic solvents without an external base led to the formation of supramolecular gels, which possess…”
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Catalytic combustion of a dendrimer containing ferrocene units with anti‐migration performance on composite propellant by Chen, Dingning, Yu, Haojie, Wang, Li, Vatsadze, Sergey Z., Liu, Jinyi, Wang, Yu

“…Ferrocene‐based compounds are promising burning rate catalysts due to their attractive catalytic activity, flammability, and non‐toxic performance…”
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A new approach to ferrocene derived alkenes via copper-catalyzed olefination by Muzalevskiy, Vasily M, Shastin, Aleksei V, Demidovich, Alexandra D, Shikhaliev, Namiq G, Magerramov, Abel M, Khrustalev, Victor N, Rakhimov, Rustem D, Vatsadze, Sergey Z, Nenajdenko, Valentine G

“…A new approach to ferrocenyl haloalkenes and bis-alkenes was elaborated. The key procedure involves copper catalyzed olefination of N-unsubstituted hydrazones,…”
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