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1,3-Difunctionalization of Alkenes by Cobaloxime Photocatalysis.
Yu, Ji-Xin; Cheng, Yuan-Yuan; Zeng, Xin-Yi; Chen, Bin; Tung, Chen-Ho; Wu, Li-Zhu.
Afiliación
  • Yu JX; Key Laboratory of Photochemical Conversion and Optoelectronic Materials, New Cornerstone Science Laboratory, Technical Institute of Physics and Chemistry, The Chinese Academy of Sciences, Beijing 100190, P. R. China.
  • Cheng YY; School of Future Technology, University of Chinese Academy of Sciences, Beijing 100049, P. R. China.
  • Zeng XY; Key Laboratory of Photochemical Conversion and Optoelectronic Materials, New Cornerstone Science Laboratory, Technical Institute of Physics and Chemistry, The Chinese Academy of Sciences, Beijing 100190, P. R. China.
  • Chen B; School of Future Technology, University of Chinese Academy of Sciences, Beijing 100049, P. R. China.
  • Tung CH; Key Laboratory of Photochemical Conversion and Optoelectronic Materials, New Cornerstone Science Laboratory, Technical Institute of Physics and Chemistry, The Chinese Academy of Sciences, Beijing 100190, P. R. China.
  • Wu LZ; School of Future Technology, University of Chinese Academy of Sciences, Beijing 100049, P. R. China.
Org Lett ; 26(32): 6809-6813, 2024 Aug 16.
Article en En | MEDLINE | ID: mdl-39102516
ABSTRACT
Represented herein is the first 1,3-difunctionalization of alkenes via photocatalysis. A single cobaloxime is used to carry out two catalytic cycles in which cobaloxime is used not only as a photocatalyst to initiate the reaction but also as a metal catalyst for the ß-H elimination process. Electron-deficient alkenes, electron-rich alkenes, and unactivated alkenes could be directly converted to 1,3-bisphosphorylated products, even unsymmetric 1,3-bisphosphorylated products, with only H2 as a byproduct under extremely mild reaction conditions.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Org Lett Asunto de la revista: BIOQUIMICA Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos