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Synthesis of Diverse Boron-Handled N-Heterocycles via Radical Borylative Cyclization of N-Allylcyanamides.
Jin, Ji-Kang; Zhang, Feng-Lian; Zhao, Qiang; Lu, Jun-An; Wang, Yi-Feng.
Afiliação
  • Jin JK; Hefei National Laboratory for Physical Sciences at the Microscale, Center for Excellence in Molecular Synthesis of CAS, and Department of Chemistry , University of Science and Technology of China , Hefei 230026 , China.
  • Zhang FL; Hefei National Laboratory for Physical Sciences at the Microscale, Center for Excellence in Molecular Synthesis of CAS, and Department of Chemistry , University of Science and Technology of China , Hefei 230026 , China.
  • Zhao Q; Hefei National Laboratory for Physical Sciences at the Microscale, Center for Excellence in Molecular Synthesis of CAS, and Department of Chemistry , University of Science and Technology of China , Hefei 230026 , China.
  • Lu JA; Hefei National Laboratory for Physical Sciences at the Microscale, Center for Excellence in Molecular Synthesis of CAS, and Department of Chemistry , University of Science and Technology of China , Hefei 230026 , China.
  • Wang YF; Hefei National Laboratory for Physical Sciences at the Microscale, Center for Excellence in Molecular Synthesis of CAS, and Department of Chemistry , University of Science and Technology of China , Hefei 230026 , China.
Org Lett ; 20(23): 7558-7562, 2018 12 07.
Article em En | MEDLINE | ID: mdl-30427202
ABSTRACT
A synthetic method based on radical borylation/cyclization cascades of N-allylcyanamides was developed to construct diverse boron-substituted N-heterocycles. In the reaction process, the N-heterocyclic carbene-boryl radical underwent a chemo- and regioselective addition to the alkene moiety, followed by cyclization with the N-cyano group. The resulting amide-iminyl radical intermediates underwent further reactions to afford various boron-tethered N-heterocyclic molecules. Further transformations to access synthetically useful building blocks were also demonstrated.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China