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Copper-catalyzed direct amination of benzylic hydrocarbons and inactive aliphatic alkanes with arylamines.
Yao, Hua; Xie, Bo; Zhong, Xiaoyang; Jin, Shengzhou; Lin, Sen; Yan, Zhaohua.
Afiliação
  • Yao H; Department of Chemistry, Nanchang University, No. 999, Xuefu Rd., Nanchang, 330031, P. R. China. senlin@ncu.edu.cn yanzh@ncu.edu.cn.
  • Xie B; Department of Chemistry, Nanchang University, No. 999, Xuefu Rd., Nanchang, 330031, P. R. China. senlin@ncu.edu.cn yanzh@ncu.edu.cn.
  • Zhong X; Department of Chemistry, Nanchang University, No. 999, Xuefu Rd., Nanchang, 330031, P. R. China. senlin@ncu.edu.cn yanzh@ncu.edu.cn.
  • Jin S; Department of Chemistry, Nanchang University, No. 999, Xuefu Rd., Nanchang, 330031, P. R. China. senlin@ncu.edu.cn yanzh@ncu.edu.cn.
  • Lin S; Department of Chemistry, Nanchang University, No. 999, Xuefu Rd., Nanchang, 330031, P. R. China. senlin@ncu.edu.cn yanzh@ncu.edu.cn.
  • Yan Z; Department of Chemistry, Nanchang University, No. 999, Xuefu Rd., Nanchang, 330031, P. R. China. senlin@ncu.edu.cn yanzh@ncu.edu.cn.
Org Biomol Chem ; 18(17): 3263-3268, 2020 05 06.
Article em En | MEDLINE | ID: mdl-32301941
ABSTRACT
A new synthetic method toward direct C-N bond formation through saturated C-H amination of benzylic hydrocarbons and inactive aliphatic alkanes with primary aromatic amines under an inexpensive catalyst/oxidant (Cu/DTBP) system has been developed. Both aminopyridines and anilines could react smoothly with primary and secondary benzylic C-H substrates or cyclohexane to form the corresponding aromatic secondary amines in moderate to good yields. This protocol has the advantages of wide functional group tolerance and use of readily available raw materials.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2020 Tipo de documento: Article