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Room-Temperature Decarboxylative Couplings of α-Oxocarboxylates with Aryl Halides by Merging Photoredox with Palladium Catalysis.
Cheng, Wan-Min; Shang, Rui; Yu, Hai-Zhu; Fu, Yao.
Afiliação
  • Cheng WM; iChEM, CAS Key Laboratory of Urban Pollutant Conversion, Anhui Province Key Laboratory of Biomass Clean Energy, Department of Chemistry, University of Science and Technology of China, Hefei 230026 (P.R. China).
  • Shang R; iChEM, CAS Key Laboratory of Urban Pollutant Conversion, Anhui Province Key Laboratory of Biomass Clean Energy, Department of Chemistry, University of Science and Technology of China, Hefei 230026 (P.R. China). faint123@mail.ustc.edu.cn.
  • Yu HZ; iChEM, CAS Key Laboratory of Urban Pollutant Conversion, Anhui Province Key Laboratory of Biomass Clean Energy, Department of Chemistry, University of Science and Technology of China, Hefei 230026 (P.R. China).
  • Fu Y; iChEM, CAS Key Laboratory of Urban Pollutant Conversion, Anhui Province Key Laboratory of Biomass Clean Energy, Department of Chemistry, University of Science and Technology of China, Hefei 230026 (P.R. China). fuyao@ustc.edu.cn.
Chemistry ; 21(38): 13191-5, 2015 Sep 14.
Article em En | MEDLINE | ID: mdl-26230749
ABSTRACT
Enabled by merging iridium photoredox catalysis and palladium catalysis, α-oxocarboxylate salts can be decarboxylatively coupled with aryl halides to generate aromatic ketones and amides at room temperature. DFT calculations suggest that this reaction proceeds through a Pd(0) -Pd(II) -Pd(III) pathway, in which the Pd(III) intermediate is responsible for reoxidizing Ir(II) to complete the Ir(III) -*Ir(III) -Ir(II) photoredox cycle.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2015 Tipo de documento: Article