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Direct synthesis of branched amines enabled by dual-catalyzed allylic C─H amination of alkenes with amines.
Ren, Yu-Feng; Chen, Bi-Hong; Chen, Xiao-Yi; Du, Hai-Wu; Li, Yu-Long; Shu, Wei.
Afiliação
  • Ren YF; Department of Chemistry, Guangming Advanced Research Institute and Shenzhen Grubbs Institute, Southern University of Science and Technology, 518055 Guangdong, P. R. China.
  • Chen BH; Department of Chemistry, Guangming Advanced Research Institute and Shenzhen Grubbs Institute, Southern University of Science and Technology, 518055 Guangdong, P. R. China.
  • Chen XY; Department of Chemistry, Guangming Advanced Research Institute and Shenzhen Grubbs Institute, Southern University of Science and Technology, 518055 Guangdong, P. R. China.
  • Du HW; Department of Chemistry, Guangming Advanced Research Institute and Shenzhen Grubbs Institute, Southern University of Science and Technology, 518055 Guangdong, P. R. China.
  • Li YL; College of Chemistry and Environmental Engineering, Sichuan University of Science and Engineering, 643000 Zigong, P. R. China.
  • Shu W; Department of Chemistry, Guangming Advanced Research Institute and Shenzhen Grubbs Institute, Southern University of Science and Technology, 518055 Guangdong, P. R. China.
Sci Adv ; 10(14): eadn1272, 2024 Apr 05.
Article em En | MEDLINE | ID: mdl-38578992
ABSTRACT
Direct conversion of hydrocarbons into amines represents an important and atom-economic goal in chemistry for decades. However, intermolecular cross-coupling of terminal alkenes with amines to form branched amines remains extremely challenging. Here, a visible-light and Co-dual catalyzed direct allylic C─H amination of alkenes with free amines to afford branched amines has been developed. Notably, challenging aliphatic amines with strong coordinating effect can be directly used as C─N coupling partner to couple with allylic C─H bond to form advanced amines with molecular complexity. Moreover, the reaction proceeds with exclusive regio- and chemoselectivity at more steric hinder position to deliver primary, secondary, and tertiary aliphatic amines with diverse substitution patterns that are difficult to access otherwise.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Sci Adv Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Sci Adv Ano de publicação: 2024 Tipo de documento: Article