Результаты исследований: Научные публикации в периодических изданиях › Обзорная статья › Рецензирование
Organofluorine chemistry : Promising growth areas and challenges. / Politanskaya, Larisa V.; Selivanova, Galina A.; Panteleeva, Elena V.; Tretyakov, Evgeny V.; Platonov, Vyacheslav E.; Nikul'Shin, Pavel V.; Vinogradov, Andrey S.; Zonov, Yaroslav V.; Karpov, Victor M.; Mezhenkova, Tatyana V.; Vasilyev, Aleksander V.; Koldobskii, Andrei B.; Shilova, Olga S.; Morozova, Sofia M.; Burgart, Yanina V.; Shchegolkov, Evgeny V.; Saloutin, Victor I.; Sokolov, Vladimir B.; Aksinenko, Aleksey Yu; Nenajdenko, Valentine G.; Moskalik, Mikhail Yu; Astakhova, Vera V.; Shainyan, Bagrat A.; Tabolin, Andrey A.; Ioffe, Sema L.; Muzalevskiy, Vasiliy M.; Balenkova, Elizaveta S.; Shastin, Alexey V.; Tyutyunov, Andrey A.; Boiko, Vladimir E.; Igumnov, Sergei M.; Dilman, Alexander D.; Adonin, Nicolay Yu; Bardin, Vadim V.; Masoud, Salekh M.; Vorobyeva, Daria V.; Osipov, Sergey N.; Nosova, Emiliya V.; Lipunova, Galina N.; Charushin, Valery N.; Prima, Darya O.; Makarov, Arkady G.; Zibarev, Andrey V.; Trofimov, Boris A.; Sobenina, Lyubov N.; Belyaeva, Kseniya V.; Sosnovskikh, Vyacheslav Ya; Obydennov, Dmitrii L.; Usachev, Sergey A.
в: Russian Chemical Reviews, Том 88, № 5, 01.01.2019, стр. 425-569.Результаты исследований: Научные публикации в периодических изданиях › Обзорная статья › Рецензирование
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TY - JOUR
T1 - Organofluorine chemistry
T2 - Promising growth areas and challenges
AU - Politanskaya, Larisa V.
AU - Selivanova, Galina A.
AU - Panteleeva, Elena V.
AU - Tretyakov, Evgeny V.
AU - Platonov, Vyacheslav E.
AU - Nikul'Shin, Pavel V.
AU - Vinogradov, Andrey S.
AU - Zonov, Yaroslav V.
AU - Karpov, Victor M.
AU - Mezhenkova, Tatyana V.
AU - Vasilyev, Aleksander V.
AU - Koldobskii, Andrei B.
AU - Shilova, Olga S.
AU - Morozova, Sofia M.
AU - Burgart, Yanina V.
AU - Shchegolkov, Evgeny V.
AU - Saloutin, Victor I.
AU - Sokolov, Vladimir B.
AU - Aksinenko, Aleksey Yu
AU - Nenajdenko, Valentine G.
AU - Moskalik, Mikhail Yu
AU - Astakhova, Vera V.
AU - Shainyan, Bagrat A.
AU - Tabolin, Andrey A.
AU - Ioffe, Sema L.
AU - Muzalevskiy, Vasiliy M.
AU - Balenkova, Elizaveta S.
AU - Shastin, Alexey V.
AU - Tyutyunov, Andrey A.
AU - Boiko, Vladimir E.
AU - Igumnov, Sergei M.
AU - Dilman, Alexander D.
AU - Adonin, Nicolay Yu
AU - Bardin, Vadim V.
AU - Masoud, Salekh M.
AU - Vorobyeva, Daria V.
AU - Osipov, Sergey N.
AU - Nosova, Emiliya V.
AU - Lipunova, Galina N.
AU - Charushin, Valery N.
AU - Prima, Darya O.
AU - Makarov, Arkady G.
AU - Zibarev, Andrey V.
AU - Trofimov, Boris A.
AU - Sobenina, Lyubov N.
AU - Belyaeva, Kseniya V.
AU - Sosnovskikh, Vyacheslav Ya
AU - Obydennov, Dmitrii L.
AU - Usachev, Sergey A.
PY - 2019/1/1
Y1 - 2019/1/1
N2 - Currently, the chemistry of organofluorine compounds is a leading and rapidly developing area of organic chemistry. The presence of fluorine largely determines specific chemical and biological properties of the molecule. This thematic issue covers the trends of organofluorine chemistry that have been actively developed in the last 1520 years in Russia. The review describes nucleophilic substitution and heterocyclization reactions involving fluorinated arenes and quinones and skeletal cationoid rearrangements in the polyfluoroarene series. The transformations involving CF3-substituted carbocations and radical cations are considered. Heterocyclization and oxidative addition reactions of trifluoroacetamide derivatives and transformations of the organic moiety in polyfluorinated organoboranes and borates with retention of the carbonboron bond are discussed. Particular attention is devoted to catalytic olefination using freons as an efficient synthetic route to fluorinated compounds. The application of unsymmetric
AB - Currently, the chemistry of organofluorine compounds is a leading and rapidly developing area of organic chemistry. The presence of fluorine largely determines specific chemical and biological properties of the molecule. This thematic issue covers the trends of organofluorine chemistry that have been actively developed in the last 1520 years in Russia. The review describes nucleophilic substitution and heterocyclization reactions involving fluorinated arenes and quinones and skeletal cationoid rearrangements in the polyfluoroarene series. The transformations involving CF3-substituted carbocations and radical cations are considered. Heterocyclization and oxidative addition reactions of trifluoroacetamide derivatives and transformations of the organic moiety in polyfluorinated organoboranes and borates with retention of the carbonboron bond are discussed. Particular attention is devoted to catalytic olefination using freons as an efficient synthetic route to fluorinated compounds. The application of unsymmetric
KW - CF3-замещенный
KW - алкен
KW - алкин
KW - арен
KW - гексафторацетон
KW - гетероциклизация
KW - диаминобензол
KW - дифторалкилирование
KW - замещение
KW - имин
KW - катализатор
KW - катионоидный
KW - метатезис
KW - метилтрифторпируват
KW - нуклеофильное
KW - органоборан
KW - пиридин
KW - пирон
KW - пиррол
KW - полифторарен
KW - полифторароматический
KW - превращения
KW - силан
KW - трифторацетамид
KW - трифторметилированный
KW - фреон
KW - фтор
KW - фторнитросоединение
KW - фторорганический
KW - химия
KW - хинолин
KW - хинон
KW - хромон
KW - CF3-замещенный
KW - алкен
KW - алкин
KW - арен
KW - гексафторацетон
KW - гетероциклизация
KW - диаминобензол
KW - дифторалкилирование
KW - замещение
KW - имин
KW - катализатор
KW - катионоидный
KW - метатезис
KW - метилтрифторпируват
KW - нуклеофильное
KW - органоборан
KW - пиридин
KW - пирон
KW - пиррол
KW - полифторарен
KW - полифторароматический
KW - превращения
KW - силан
KW - трифторацетамид
KW - трифторметилированный
KW - фреон
KW - фтор
KW - фторнитросоединение
KW - фторорганический
KW - химия
KW - хинолин
KW - хинон
KW - хромон
UR - http://www.scopus.com/inward/record.url?scp=85066251313&partnerID=8YFLogxK
UR - http://www.mendeley.com/research/organofluorine-chemistry-promising-growth-areas-challenges
U2 - 10.1070/RCR4871
DO - 10.1070/RCR4871
M3 - Review article
AN - SCOPUS:85066251313
VL - 88
SP - 425
EP - 569
JO - Russian Chemical Reviews
JF - Russian Chemical Reviews
SN - 0036-021X
IS - 5
ER -
ID: 44001285