Radical Nitration-Debromination of α-Bromo-α-fluoroalkenes as a Stereoselective Route to Aromatic α-Fluoronitroalkenes—Functionalized Fluorinated Building Blocks for Organic Synthesis Научная публикация
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Journal of Organic Chemistry
ISSN: 1520-6904 , E-ISSN: 0022-3263 |
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| Вых. Данные | Год: 2017, Том: 82, Номер: 10, Страницы: 5274-5284 Страниц : 11 DOI: 10.1021/acs.joc.7b00578 | ||||||||||
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Реферат:
A new highly efficient method for the synthesis of 2-fluoro-2-nitrostyrenes was described. Radical nitration of readily available 2-bromo-2-fluorostyrenes with Fe(NO3)3·9H2O resulted in the formation of the corresponding α-fluoro-nitroalkenes in isolated yields up to 92%. The reaction proceeded as a nitration-debromination sequence to highly stereoselectively give α-fluoro-nitroalkenes as Z-isomers only. The broad scope of this method was demonstrated. Prepared monofluorinated alkenes were shown to be versatile building blocks for the synthesis of various fluorinated products.
Библиографическая ссылка:
Motornov V.A.
, Muzalevskiy V.M.
, Tabolin A.A.
, Novikov R.A.
, Nelyubina Y.V.
, Nenajdenko V.G.
, Ioffe S.L.
Radical Nitration-Debromination of α-Bromo-α-fluoroalkenes as a Stereoselective Route to Aromatic α-Fluoronitroalkenes—Functionalized Fluorinated Building Blocks for Organic Synthesis
Journal of Organic Chemistry. 2017. V.82. N10. P.5274-5284. DOI: 10.1021/acs.joc.7b00578 WOS Scopus OpenAlex
Radical Nitration-Debromination of α-Bromo-α-fluoroalkenes as a Stereoselective Route to Aromatic α-Fluoronitroalkenes—Functionalized Fluorinated Building Blocks for Organic Synthesis
Journal of Organic Chemistry. 2017. V.82. N10. P.5274-5284. DOI: 10.1021/acs.joc.7b00578 WOS Scopus OpenAlex
Идентификаторы БД:
| ≡ Web of science: | WOS:000402023200027 |
| ≡ Scopus: | 2-s2.0-85019367997 |
| ≡ OpenAlex: | W2607925707 |