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Catalyst-Free Arylation of Tertiary Phosphines with Diaryliodonium Salts Enabled by Visible Light.
Bugaenko, Dmitry I; Volkov, Alexey A; Livantsov, Mikhail V; Yurovskaya, Marina A; Karchava, Alexander V.
Afiliação
  • Bugaenko DI; Department of Chemistry, M. V. Lomonosov Moscow State University, 119234, Moscow, Russia.
  • Volkov AA; Department of Chemistry, M. V. Lomonosov Moscow State University, 119234, Moscow, Russia.
  • Livantsov MV; Department of Chemistry, M. V. Lomonosov Moscow State University, 119234, Moscow, Russia.
  • Yurovskaya MA; Department of Chemistry, M. V. Lomonosov Moscow State University, 119234, Moscow, Russia.
  • Karchava AV; Department of Chemistry, M. V. Lomonosov Moscow State University, 119234, Moscow, Russia.
Chemistry ; 25(54): 12502-12506, 2019 Sep 25.
Article em En | MEDLINE | ID: mdl-31339601
The visible-light-induced arylation of tertiary phosphines with aryl(mesityl)iodonium triflates to produce the quaternary phosphonium salts occurs under mild, metal, and catalyst-free conditions. Photo-excited EDA complexes between diaryliodonium salts and phosphines supposedly enable this transformation, which is difficult to achieve through the traditional ground-state reactions. Demonstrating high functional group tolerance, broad scope, and complete selectivity of the aryl group transfer, the method is particularly compatible with sterically congested phosphines, which are challenging under metal-based catalytic methods.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article