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AgNTf2-Catalyzed Regioselective C-H Alkenylation of N,N-Dialkylanilines with Ynamides.
Nie, Xiao-Di; Mao, Zhuo-Ya; Guo, Jia-Ming; Si, Chang-Mei; Wei, Bang-Guo; Lin, Guo-Qiang.
Afiliação
  • Nie XD; School of Pharmacy and Institutes of Biomedical Sciences, Fudan University, 826 Zhangheng Road, Shanghai 201203, China.
  • Mao ZY; School of Pharmacy and Institutes of Biomedical Sciences, Fudan University, 826 Zhangheng Road, Shanghai 201203, China.
  • Guo JM; School of Pharmacy and Institutes of Biomedical Sciences, Fudan University, 826 Zhangheng Road, Shanghai 201203, China.
  • Si CM; School of Pharmacy and Institutes of Biomedical Sciences, Fudan University, 826 Zhangheng Road, Shanghai 201203, China.
  • Wei BG; School of Pharmacy and Institutes of Biomedical Sciences, Fudan University, 826 Zhangheng Road, Shanghai 201203, China.
  • Lin GQ; Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.
J Org Chem ; 87(5): 2380-2392, 2022 03 04.
Article em En | MEDLINE | ID: mdl-35041783
ABSTRACT
Regioselective C-H alkenylation of N,N-dialkylanilines with ynamides was developed using AgNTf2 as a catalyst. This approach represents a facile hydroarylation of ynamides, allowing for the introduction of an alkenyl group exclusively at the para position of aniline derivatives. As a result, a series of 4-alkenyl N,N-dialkylanilines were synthesized with excellent regioselectivities.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Catálise Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Catálise Idioma: En Ano de publicação: 2022 Tipo de documento: Article