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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  • 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
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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
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  • 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
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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
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  • 2011 A route to diffusion embedding of CdSe/CdS quantum dots in fluoropolymer microparticles
  • Popov V.K., Bagratashvili V.N., Krotova L.I., Rybaltovskii A.O., Smith D.C., Timashev P.S., Yang J., Zavorotnii Yu S., Howdle S.M.
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 13, № 10, с. 2696-2700 DOI
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  • 2011 Ionic liquids based on the imidazolium cation in platinum and titanium electropolishing
  • Lebedeva O., Jungurova G., Kultin D., Kustov L., Zakharov A., Kalmikov K., Chernikova E., Krasovskiy V.
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 13, № 4, с. 1004-1008 DOI
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  • 2011 NMR Analysis of Chiral Alcohols and Amines: Development of Environmentally Benign "In Tube" Procedure with High Efficiency and Improved Detection Limit
  • Orlov N.V., Ananikov V.P.
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 13, с. 1735-1744 DOI
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  • 2010 Ionic liquids based on imidazolium tetrafluoroborate for the removal of aromatic sulfur-containing compounds from hydrocarbon mixtures
  • Lebedeva O., Kultin D., Kustov L., Borisenkova S., Krasovskiy V., Nefedieva M.
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 12, № 2, с. 346-349 DOI
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  • 2008 A green, fully enzymatic procedure for amine resolution, using a lipase and a penicillin G acylase
  • Ismail Hilda, Lau Rute Madeira, van Langen Luuk M., van Rantwijk Fred, Svedas Vytas K., Sheldon Roger A.
  • в журнале Green Chemistry, издательство Royal Society of Chemistry (United Kingdom), том 10, № 4, с. 415-418