Reactions of gem-Difluorinated Phosphonium Salts Induced by Light Научная публикация
Журнал |
Organic Letters
ISSN: 1523-7060 , E-ISSN: 1523-7052 |
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Вых. Данные | Год: 2016, Том: 18, Номер: 5, Страницы: 996-999 Страниц : 4 DOI: 10.1021/acs.orglett.6b00117 | ||||
Авторы |
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Реферат:
gem-Difluorinated phosphonium salts, which are readily obtained from aldehydes and difluoromethylene phosphobetaine, can serve as a source of radicals under reductive conditions. An iridium complex or Hantzsch ester was used as a one-electron reducing agent when irradiated with visible light. The fluorinated radicals were trapped with various alkenes, leading to products either via a photoredox cycle (for the iridium catalyst) or via a hydrogen atom transfer (for the Hantzsch ester).
Библиографическая ссылка:
Panferova L.I.
, Tsymbal A.V.
, Levin V.V.
, Struchkova M.I.
, Dilman A.D.
Reactions of gem-Difluorinated Phosphonium Salts Induced by Light
Organic Letters. 2016. V.18. N5. P.996-999. DOI: 10.1021/acs.orglett.6b00117 Scopus OpenAlex
Reactions of gem-Difluorinated Phosphonium Salts Induced by Light
Organic Letters. 2016. V.18. N5. P.996-999. DOI: 10.1021/acs.orglett.6b00117 Scopus OpenAlex
Идентификаторы БД:
Scopus: | 2-s2.0-84960157688 |
OpenAlex: | W2331899840 |