Green Chemistryжурнал

Редколлегия

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• Тарасова Наталия Павловна, с 30 ноября 2015
• Бумагин Николай Александрович, с 1 марта 2013

Статьи, опубликованные в журнале

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• • 2023 Advanced Research and Prospects on Polymer Ionic Liquids: Trends, Potential and Application
  • Lebedeva Olga, Kultin Dmitry, Kustov Leonid
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 25, № 22, с. 9001-9019 DOI
• • 2023 Empowering strategies of electrochemical N–N bond forming reactions: direct access to previously neglected 1,2,3-triazole 1-oxides
  • Titenkova Kseniia, Shuvaev Alexander D., Teslenko Fedor E., Zhilin Egor S., Fershtat Leonid L.
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom) DOI
• • 2023 Rapid access to molecular complexity from bioderived 5-HMF derivatives $\less$i$\greater$via$\less$/i$\greater$ cascade cycloadditions
  • Averochkin Gleb M., Gordeev Evgeniy G., Kucherov Fedor A., Ananikov Valentine P.
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 25, № 3, с. 1045-1055 DOI
• • 2022 Fabrication of a hollow sphere N, S co-doped bifunctional carbon catalyst for sustainable fixation of CO2 to cyclic carbonates
  • Ghosh Anindya, Reddy G.Naaresh, K Mohammed Siddhique P., Chatterjee Sauvik, Bhattacharjee Sudip, Maitra Rahul, Lyubimov Sergey Evgenevich, Arzumanyan Ashot Vachikovich, Naumkin Alexander, Bhaumik Asim, Chowdhury Biswajit
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom) DOI
• • 2022 Switchable light vs. acid-induced transformations of complex framework compounds at room temperature
  • Kobzev M.S., Titov A.A., Borisova T.N., Voskressensky L.G., Varlamov A.V., D’Alterio M.C., Petrone A., Luque R., Talarico G.
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom) DOI
• • 2021 A large-scale study of ionic liquids employed in chemistry and energy research to reveal cytotoxicity mechanisms and to develop safe design guide
  • Dzhemileva Lilya U., D'yakonov Vladimir Anatolievich, Seitkalieva Marina M., Kulikovskaya Natalia, Egorova Ksenia S., Ananikov Valentine
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom) DOI
• • 2021 Biomass- and calcium carbide-based recyclable polymers
  • Metlyaeva Svetlana A., Rodygin Konstantin S., Lotsman Kristina A., Samoylenko Dmitriy E., Ananikov Valentine P.
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom) DOI
• • 2021 Building bio-Profiles for common catalytic reactions
  • Egorova Ksenia S., Galushko Alexey S., Dzhemileva Lilya U., D′yakonov Vladimir A., Ananikov Valentine P.
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom) DOI
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  • 2021 Oxo-functionalised mesoionic NHC nickel complexes for selective electrocatalytic reduction of CO2 to formate
  • Bertini Simone, Rahaman Motiar, Dutta Abhijit, Schollhammer Philippe, Rudnev Alexander V., Gloaguen Fredric, Broekmann Peter, Albrecht Martin
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 23, № 9, с. 3365-3373 DOI
• • 2020 Hierarchical Beta zeolites as catalysts in a one-pot three-component cascade Prins–Friedel–Crafts reaction
  • Barakov Roman, Shcherban Nataliya, Yaremov Pavel, Bezverkhyy Igor, Čejka Jiří, Opanasenko Maksym
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 22, № 20, с. 6992-7002 DOI
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  • 2019 A tunable precious metal-free system for selective oxidative esterification of biobased 5-(hydroxymethyl)furfural
  • Kozlov Kirill S., Romashov Leonid V., Ananikov Valentine P.
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 21, № 12, с. 3464-3468 DOI
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  • 2019 Diastereoselective synthesis of CF3-oxazinoquinolines in water
  • Muzalevskiy Vasiliy M., Belyaeva Kseniya V., Trofimov Boris A., Nenajdenko Valentine G.
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 21, № 23, с. 6353-6360 DOI
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  • 2019 Hydrazo coupling: the efficient transition-metal-free C–H functionalization of 8-hydroxyquinoline and phenol through base catalysis
  • Solyev Pavel N., Sherman Daria K., Novikov Roman A., Levina Eugenia A., Kochetkov Sergey N.
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 21, № 23, с. 6381-6389 DOI
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  • 2019 Oxidation of a wood extractive betulin to biologically active oxo-derivatives using supported gold catalysts
  • Kolobova E.N., Pakrieva E.G., Carabineiro S.A.C, Bogdanchikova N., Kharlanov A.N., Kazantsev S.O., Hemming J., Mäki-Arvela P., Pestryakov A.N., Murzin D.Yu
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 21, с. 3370-3382 DOI
• • 2018 Aerobic Co or Cu / NHPI - catalyzed oxidation of hydride siloxanes: synthesis of siloxanols
  • Arzumanyan Ashot V., Goncharova Irina K., Novikov Roman A., Milenin Sergey, Boldyrev Konstantin L., Solyev Pavel N., Volodin Alexander D., Smol’yakov Alexander F., Korlyukov Aleksander, Muzafarov Aziz
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom) DOI
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  • 2018 Chapter 2: Catalytic processes and catalyst development in biorefining
  • Taran O.P., Gromov N.V., Parmon V.N.
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 56, с. 25-64 DOI
• • 2018 Mechanochemistry – a new powerful green approach to direct synthesis of alkoxysilanes
  • Temnikov Maxim, Anisimov Anton, Zhemchugov Pavel, Kholodkov Dmitry, Goloveshkin Alexander S., Naumkin Alexander, Chistovalov Sergey, Katsulis Dimitris E., Muzafarov Aziz
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom) DOI
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  • 2017 A solid acetylene reagent with enhanced reactivity: fluoride-mediated functionalization of alcohols and phenols
  • Werner Georg, Rodygin Konstantin S., Kostin Anton A., Gordeev Evgeniy G., Kashin Alexey S., Ananikov Valentine P.
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 19, № 13, с. 3032-3041 DOI
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  • 2017 Efficient route for the construction of polycyclic systems from bioderived HMF
  • Kucherov F.A., Galkin K.I., Gordeev E.G., Ananikov V.P.
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 19, № 20, с. 4858-4864 DOI
• • 2017 Enzymatic surface hydrolysis of poly(ethylene furanoate) thin films of various crystallinities
  • Weinberger S., Haernvall K., Scaini D., Ghazaryan G., Zumstein M.T., Sander M., Pellis A., Guebitz G.M.
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 19, № 22, с. 5381-5384 DOI
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  • 2016 An efficient metal-free pathway to vinyl thioesters with calcium carbide as the acetylene source
  • Rodygin K.S., Ananikov V.P.
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 18, № 2, с. 482-486 DOI
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  • 2016 Unprecedentedly Simple Method of Synthesis of Aryl Azides and 3-Hydroxytriazenes
  • Gribanov Pavel, Topchiy Maxim, Golenko Yulia, Lichtenstein Yana, Eshtukov Artur, Terekhov Vladimir, Asachenko Andrey, Nechaev Mikhail
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 18, с. 5984-5988 DOI
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  • 2015 Ethanol conversion into butadiene over Zr-containing molecular sieves doped with silver
  • Sushkevich Vitaly L., Ivanova Irina I., Taarning Esben
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 17, № 4, с. 2552-2559 DOI
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  • 2015 Glycine catalyzed diastereoselective domino-synthesis of 6-imino-2,7-dioxabicyclo[3.2.1]-octane-4,4,5-tricarbonitriles in water
  • Ershov O.V., Ievlev M.Yu, Tafeenko V.A., Nasakin O.E.
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 17, № 8, с. 4234-4238 DOI
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  • 2014 Synthesis of polyacrylonitrile copolymers as potential carbon fibre precursors in CO2
  • Shlyahtin Andrei V., Nifant'ev Ilya E., Bagrov Vladimir V., Lemenovskii Dmitrii A., Tavtorkin Aleksander N., Timashev Peter S.
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 16, № 3, с. 1344-1350 DOI