Organic Chemistry Frontiersжурнал

Статьи, опубликованные в журнале

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  • 2024 Ring expansion of unsubstituted aziridinium ylides to trifluoromethylated dehydropiperidines
  • Tang Jiaqi, Tian Tian, Wang Yingyu, Wei Dandan, Yang Yong, Wang Xinyu, Sivaguru Paramasivam, Ning Yongquan, Liu Zhaohong, Nenajdenko Valentine
  • в журнале Organic Chemistry Frontiers DOI
• • 2023 Atom-economical synthesis of 1,2-bis(phosphine oxide)ethanes from calcium carbide with straightforward access to deuterium- and $\less$sup$\greater$13$\less$/sup$\greater$C-labeled bidentate phosphorus ligands and metal complexes
  • Lotsman Kristina A., Rodygin Konstantin S., Skvortsova Irina, Kutskaya Anastasia M., Minyaev Mikhail E., Ananikov Valentine P.
  • в журнале Organic Chemistry Frontiers, том 10, № 4, с. 1022-1033 DOI
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  • 2023 Atom-economical synthesis of 1,2-bis(phosphine oxide)ethanes from calcium carbide with straightforward access to deuterium- and ¹³C-labeled bidentate phosphorus ligands and metal complexes
  • Lotsman Kristina A., Rodygin Konstantin S., Skvortsova Irina, Kutskaya Anastasia M., Minyaev Mikhail E., Ananikov Valentine P.
  • в журнале Organic Chemistry Frontiers, том 10, № 4, с. 1022-1033 DOI
• • 2023 Diacetyliminoxyl as a selective radical reagent for organic synthesis: dehydrogenation and dehydrogenative C–O coupling reactions
  • Budnikov Alexander S., Krylov Igor B., Kuzmin Ilya V., Segida Oleg O., Lastovko Andrey V., Shevchenko Mikhail I., Nikishin Gennady I., Terent'ev Alexander O.
  • в журнале Organic Chemistry Frontiers, том 10, № 2, с. 388-398 DOI
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  • 2023 Disulfides as versatile starting reagents: effective sulfonylation of alkenes with disulfides under electrochemical conditions
  • Mulina Olga M., Doronin Mikhail M., He Liang-Nian, Terent'ev Alexander O.
  • в журнале Organic Chemistry Frontiers, том 10, № 14, с. 3559-3566 DOI
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  • 2023 Enriching calixarene functionality with 1,3-diketone groups
  • Sakovich Maria, Sokolova Daria, Alekseev Ivan, Lentin Ivan, Gorbunov Alexander, Malakhova Maria, Ershov Ivan, Zairov Rustem, Korniltsev Ilia, Podyachev Sergey, Bezzubov Stanislav, Kovalev Vladimir, Vatsouro Ivan
  • в журнале Organic Chemistry Frontiers, том 10, № 14, с. 3619-3636 DOI
• • 2023 Shrinkable/stretchable bis(calix[4]arenes) comprising photoreactive azobenzene or stilbene linkers
  • Lentin Ivan, Gorbunov Alexander, Bezzubov Stanislav, Nosova Valentina, Cheshkov Dmitry, Kovalev Vladimir, Vatsouro Ivan
  • в журнале Organic Chemistry Frontiers, том 10, № 6, с. 1470-1484 DOI
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  • 2022 Recent advances in the application of ylide-like species in [4 + 1]-annulation reactions: an updated review
  • Ushakov Pavel Yu, Ioffe Sema L., Sukhorukov Alexey Yu
  • в журнале Organic Chemistry Frontiers, том 9, № 19, с. 5358-5382 DOI
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  • 2022 Tandem Michael addition/elimination – novel reactivity of pyridinium ylides in reaction with electron-deficient alkenes
  • Izmest'ev Alexei N., Motornov Vladimir A., Vinogradov Dmitry B., Ioffe Sema L., Kravchenko Angelina N., Gazieva Galina A.
  • в журнале Organic Chemistry Frontiers, том 9, № 18, с. 4998-5004 DOI
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  • 2022 The extended Corey-Chaykovsky reactions: transformation of 2-hydroxychalcones to benzannulated 2,8-dioxabicyclo[3.2.1]octanes and 2,3-dihydrobenzofurans
  • Fadeev A.A., Makarov A.S., Ivanova O.A., Uchuskin M.G., Trushkov I.V.
  • в журнале Organic Chemistry Frontiers, том 9, № 3, с. 737-744 DOI
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  • 2022 Triazolated calix[4]semitubes: assembling strategies towards long multicalixarene architectures
  • Malakhova Maria, Gorbunov Alexander, Ozerov Nikolay, Korniltsev Ilia, Ermolov Kirill, Bezzubov Stanislav, Kovalev Vladimir, Vatsouro Ivan
  • в журнале Organic Chemistry Frontiers, том 9, № 11, с. 3084-3092 DOI
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  • 2021 Assembling triazolated calix[4]semitubes by means of copper(I)-catalyzed azide–alkyne cycloaddition
  • Gorbunov Alexander, Ozerov Nikolay, Malakhova Maria, Eshtukov Artur, Cheshkov Dmitry, Bezzubov Stanislav, Kovalev Vladimir, Vatsouro Ivan
  • в журнале Organic Chemistry Frontiers, том 8, № 14, с. 3853-3866 DOI
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  • 2021 Hybrid phosphorus-viologen dendrimers as new soft nanoparticles: Design and properties
  • Majoral J.P., Zablocka M., Ciepluch K., Milowska K., Bryszewska M., Shcharbin D., Katir N., El Kadib A., Caminade A.M., Mignani S.
  • в журнале Organic Chemistry Frontiers, том 8, № 16, с. 4607-4622 DOI
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  • 2021 Ni/NHC catalysis in C–H functionalization using air-tolerant nickelocene and sodium formate for in situ catalyst generation
  • Khazipov Oleg V., Shepelenko Konstantin E., Pasyukov Dmitry V., Chesnokov Vasilii V., Soliev Safarmurod B., Chernyshev Victor M., Ananikov Valentine P.
  • в журнале Organic Chemistry Frontiers, том 8, № 11, с. 2515-2524 DOI
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  • 2020 Efficient labeling of organic molecules using 13C elemental carbon: universal access to 13C2-labeled synthetic building blocks, polymers and pharmaceuticals
  • Ledovskaya Maria S., Voronin Vladimir V., Rodygin Konstantin S., Ananikov Valentine P.
  • в журнале Organic Chemistry Frontiers, том 7, № 4, с. 638-647 DOI
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  • 2020 Examining the vinyl moiety as a protecting group for hydroxyl (–OH) functionality under basic conditions
  • Voronin Vladimir V., Ledovskaya Maria S., Rodygin Konstantin S., Ananikov Valentine P.
  • в журнале Organic Chemistry Frontiers, том 7, № 11, с. 1334-1342 DOI
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  • 2020 Folding of fluorinated oligoarylenes into non-alternant PAHs with various topological shapes
  • Akhmetov V., Förtsch A., Feofanov M., Troyanov S.I., Amsharov K.
  • в журнале Organic Chemistry Frontiers, том 7, с. 1271-1275 DOI
• • 2020 Iodine-promoted synthesis of pyrazoles from 1,3-dicarbonyl compounds and oxamic acid thiohydrazides
  • Komendantova Anna S., Lyssenko Konstantin A., Zavarzin Igor V., Volkova Yulia A.
  • в журнале Organic Chemistry Frontiers DOI
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  • 2020 Selective azide–alkyne cycloaddition reactions of azidoalkylated calixarenes
  • Gorbunov Alexander, Kuznetsova Julia, Deltsov Ilya, Molokanova Anastasia, Cheshkov Dmitry, Bezzubov Stanislav, Kovalev Vladimir, Vatsouro Ivan
  • в журнале Organic Chemistry Frontiers, том 7, № 17, с. 2432-2441 DOI
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  • 2019 3,3-Diazidoenones – new types of highly reactive bis-azides. Preparation and synthetic transformations
  • Lemport P.S., Smolyar I.V., Khrustalev V.N., Roznyatovsky V.A., Popov A.V., Kobelevskaya V.A., Rozentsveig I.B., Nenajdenko V.G.
  • в журнале Organic Chemistry Frontiers, том 6, с. 335-341 DOI
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  • 2019 A General Synthesis of Unnatural α-Amino Acids by Iron-Catalysed Olefin-Olefin Coupling via Generated Radicals
  • Larionov Vladimir A., Stoletova Nadezhda V., Kovalev Vladislav I., Smol’yakov Alexander F., Savel’yeva Tat’yana F., Maleev Victor I.
  • в журнале Organic Chemistry Frontiers, том 6, № 8, с. 1094-1099 DOI
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  • 2019 Constructing bridged multifunctional calixarenes by intramolecular indole coupling
  • Boris Bolshchikov, Sergey Volkov, Daria Sokolova, Alexander Gorbunov, Alina Serebryannikova, Gloriozov Igor, Dmitry Cheshkov, Stanislav Bezzubov, Wen-Sheng Chung, Vladimir Kovalev, Ivan Vatsouro
  • в журнале Organic Chemistry Frontiers, том 6, № 19, с. 3327-3341 DOI
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  • 2019 General approach to 2-fluoroalkyl 1,3-azoles via the tandem ring opening and defluorinative annulation of N-fluoroalkyl-1,2,3-triazoles
  • Motornov Vladimir, Kostal Vojtech, Markos Athanasios, Taffner Dominik, Beier Petr
  • в журнале Organic Chemistry Frontiers, том 6, № 22, с. 3776-3780 DOI
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  • 2019 N-(2-Fluoro-2,2-dinitroethyl)azoles: a novel assembly of diverse explosophoric building blocks for energetic compound design
  • Palysaeva Nadezhda V., Gladyshkin Aleksei G., Vatsadze Irina A., Suponitsky Kyrill Yu, Dmitriev Dmitry E., Sheremetev Aleksei B.
  • в журнале Organic Chemistry Frontiers, том 6, № 2, с. 249-255 DOI
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  • 2019 Oxalamide-based bisdiamidophosphites: synthesis, coordination, and application in asymmetric metallocatalysis
  • Gavrilov Konstantin N., Mikhel Igor S., Zheglov Sergey V., Gavrilov Vladislav K., Chuchelkin Ilya V., Firsin Ilya D., Birin Kirill P., Pytskii Ivan S., Paseshnichenko Ksenia A., Tafeenko Victor A., Chernyshev Vladimir V., Shiryaev Alexei A.
  • в журнале Organic Chemistry Frontiers, том 6, № 10, с. 1637-1648 DOI