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Cobalt-catalyzed intramolecular decarbonylative coupling of acylindoles and diarylketones through the cleavage of C-C bonds.
Yu, Tian-Yang; Xu, Wen-Hua; Lu, Hong; Wei, Hao.
Afiliación
  • Yu TY; Key Laboratory of Synthetic and Natural Functional Molecule of Ministry of the Education, College of Chemistry & Materials Science, Northwest University Xi'an 710069 China haow@nwu.edu.cn.
  • Xu WH; Key Laboratory of Synthetic and Natural Functional Molecule of Ministry of the Education, College of Chemistry & Materials Science, Northwest University Xi'an 710069 China haow@nwu.edu.cn.
  • Lu H; Key Laboratory of Synthetic and Natural Functional Molecule of Ministry of the Education, College of Chemistry & Materials Science, Northwest University Xi'an 710069 China haow@nwu.edu.cn.
  • Wei H; Key Laboratory of Synthetic and Natural Functional Molecule of Ministry of the Education, College of Chemistry & Materials Science, Northwest University Xi'an 710069 China haow@nwu.edu.cn.
Chem Sci ; 11(45): 12336-12340, 2020 Oct 16.
Article en En | MEDLINE | ID: mdl-34094442
ABSTRACT
We report here cobalt-N-heterocyclic carbene catalytic systems for the intramolecular decarbonylative coupling through the chelation-assisted C-C bond cleavage of acylindoles and diarylketones. The reaction tolerates a wide range of functional groups such as alkyl, aryl, and heteroaryl groups, giving the decarbonylative products in moderate to excellent yields. This transformation involves the cleavage of two C-C bonds and formation of a new C-C bond without the use of noble metals, thus reinforcing the potential application of decarbonylation as an effective tool for C-C bond formation.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Sci Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Sci Año: 2020 Tipo del documento: Article