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[Cu]/NFSI-Mediated Cascade Diels-Alder Radical Annulations Using Norbornene as H-Acceptor under Redox-Neutral Conditions.
Xu, Zhengyu; Weng, Jianqiao; Wei, Li; Huang, Tianming; Wu, Jie; Chen, Zhiyuan.
Afiliação
  • Xu Z; College of Chemistry & Chemical Engineering, Jiangxi Normal University, 330022 Nanchang, China.
  • Weng J; Key Laboratory of Novel Targets and Drug Study for Neural Repair of Zhejiang Province, School of Medicine, Hangzhou City University, 310015 Hangzhou, Zhejiang, China.
  • Wei L; College of Chemistry & Chemical Engineering, Jiangxi Normal University, 330022 Nanchang, China.
  • Huang T; College of Chemistry & Chemical Engineering, Jiangxi Normal University, 330022 Nanchang, China.
  • Wu J; Institute for Advanced Studies, Taizhou University, 318000 Taizhou, Zhejiang, China.
  • Chen Z; Key Laboratory of Novel Targets and Drug Study for Neural Repair of Zhejiang Province, School of Medicine, Hangzhou City University, 310015 Hangzhou, Zhejiang, China.
J Org Chem ; 89(4): 2264-2271, 2024 Feb 16.
Article em En | MEDLINE | ID: mdl-38291972
ABSTRACT
An oxidative cascade [4 + 2] radical cycloaddition/dehydroaromatization reaction of aryl alkenes to access α-aryl substituted naphthalenes under redox-neutral conditions was achieved. This reaction was found to require the addition of [Cu] catalyst along with stoichiometric concentrations of NFSI as a trigger of radical series of steps. Norbornene (NBE), rather than the conventional oxidant, manifested optimal performances as a H-acceptor in this procedure. The results herein might shed encouraging insight into the transition-metal-catalyzed dehydrogenative C-H activation protocols.

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

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