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Copper-Catalyzed Alkylarylation of Unactivated Alkenes: Synthesis of 3-Alkyl Indolines from N-Allyl Anilines and Alkanes.
Liang, Deqiang; Huo, Bojie; Dong, Yongrui; Wang, Yan; Dong, Ying; Wang, Baoling; Ma, Yinhai.
Afiliação
  • Liang D; Department of Chemistry, Kunming University, 2 Puxin Road, Kunming, Yunnan Province, 650214, China.
  • Huo B; Department of Chemistry, Kunming University, 2 Puxin Road, Kunming, Yunnan Province, 650214, China.
  • Dong Y; Department of Chemistry, Kunming University, 2 Puxin Road, Kunming, Yunnan Province, 650214, China.
  • Wang Y; Department of Chemistry, Kunming University, 2 Puxin Road, Kunming, Yunnan Province, 650214, China.
  • Dong Y; College of Chemistry, Chemical Engineering and Materials Science, Shandong Normal University, Jinan, Shandong Province, 250014, China.
  • Wang B; Yunnan Engineering Technology Research Center for Plastic Films, Kunming, Yunnan Province, 650214, China.
  • Ma Y; Department of Chemistry, Kunming University, 2 Puxin Road, Kunming, Yunnan Province, 650214, China.
Chem Asian J ; 14(11): 1932-1936, 2019 Jun 03.
Article em En | MEDLINE | ID: mdl-31046195
ABSTRACT
A rare example of C(sp3 )-H functionalization of simple alkanes with unactivated alkenes is presented. In the presence of a copper salt and di-tert-butyl peroxide (DTBP), N-allyl anilines underwent exo-selective alkylation/cyclization cascade with unactivated alkenic bonds as radical acceptors and simple alkanes as radical precursors, providing a direct access to 3-alkyl indolines. The present protocol features simple operation, broad substrate scope and great exo selectivity.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Chem Asian J Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Chem Asian J Ano de publicação: 2019 Tipo de documento: Article País de afiliação: China