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Deoxygenative Cross-Coupling of Aromatic Amides with Polyfluoroarenes.
He, Youliang; Wang, Yuxiao; Li, Shi-Jun; Lan, Yu; Wang, Xiaoming.
Afiliación
  • He Y; State Key Laboratory of Organometallic Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai, 200032, China.
  • Wang Y; State Key Laboratory of Organometallic Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai, 200032, China.
  • Li SJ; Green Catalysis Center, and College of Chemistry, Zhengzhou University, Zhengzhou, 450001, China.
  • Lan Y; Green Catalysis Center, and College of Chemistry, Zhengzhou University, Zhengzhou, 450001, China.
  • Wang X; School of Chemistry and Chemical Engineering, Chongqing Key Laboratory of Theoretical and Computational Chemistry, Chongqing University, Chongqing, 400030, China.
Angew Chem Int Ed Engl ; 61(11): e202115497, 2022 03 07.
Article en En | MEDLINE | ID: mdl-35014163
ABSTRACT
Considering the ubiquitous nature and ready synthesis of amides, and the great significance of organofluorine-containing species, the cross-coupling of amides and polyfluoroarenes, leading to new carbon-carbon bond-forming methodologies, would find useful applications in synthesis, late-stage functionalization, and rapid generation of molecular diversity. Herein, we present a novel synthesis of α-polyfluoroaryl amines via Sm/SmI2 -mediated deoxygenative cross-coupling of aromatic amides with polyfluoroarenes through direct C-H functionalization. The structural and functional diversity of these readily available precursors provides a versatile and flexible strategy for the streamlined synthesis of α-polyfluoroaryl amines. Combining experimental and theoretical studies, a novel plausible mechanism of the α-aminocarbene-mediated C-H insertion has been revealed, which may stimulate future work for the development of novel methods in amine synthesis.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2022 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Angew Chem Int Ed Engl Año: 2022 Tipo del documento: Article País de afiliación: China