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Palladium/norbornene-catalyzed diversified trifunctionalization of aryl-thianthreniums.
Nan, Jiang; Lei, Min; Chen, Gaoyang; Ma, Yangmin; Liang, Chengyuan; Wang, Jing.
Afiliação
  • Nan J; College of Chemistry and Chemical Engineering, Shaanxi University of Science and Technology, Xi'an 710021, China. nanjiang@sust.edu.cn.
  • Lei M; College of Chemistry and Chemical Engineering, Shaanxi University of Science and Technology, Xi'an 710021, China. nanjiang@sust.edu.cn.
  • Chen G; College of Chemistry and Chemical Engineering, Shaanxi University of Science and Technology, Xi'an 710021, China. nanjiang@sust.edu.cn.
  • Ma Y; College of Chemistry and Chemical Engineering, Shaanxi University of Science and Technology, Xi'an 710021, China. nanjiang@sust.edu.cn.
  • Liang C; Xi'an Key Laboratory of Antiviral and Antimicrobial-Resistant Bacteria Therapeutics Research, School of Food and Biological Engineering, Shaanxi University of Science and Technology, Xi'an 710021, China.
  • Wang J; College of Chemistry and Chemical Engineering, Shaanxi University of Science and Technology, Xi'an 710021, China. nanjiang@sust.edu.cn.
Chem Commun (Camb) ; 60(42): 5558-5561, 2024 May 21.
Article em En | MEDLINE | ID: mdl-38712611
ABSTRACT
A novel Catellani-type conversion is reported using aryl-thianthreniums (aryl-TTs) instead of aryl halides. Three classes of ortho-dual C-H functionalization involving alkylation, amination, and deuterated methylation and five types of ipso-operation including alkenylation, cyanation, methylation, hydrogenation, and alkynylation all proceed well in this procedure. In this conversion, aryl-TTs exhibit satisfactory reactivity and feature the advantage that the leaving TT unit can be recovered. More strikingly, this finding represents a new chemistry conversion of aryl-TTs, wherein contiguous tri-functionalization in a single chemical manipulation is realized.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Commun (Camb) Assunto da revista: QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chem Commun (Camb) Assunto da revista: QUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China