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Ecofriendly Protocol for ipso-Bromination of Arylboronic Acids.
Zhou, Yiqin; Akkarasereenon, Kornkamon; Liu, Lifang; Lin, Ran; Song, Liyan; Tong, Rongbiao.
Afiliação
  • Zhou Y; Department of Chemistry, The Hong Kong University of Science and Technology, Clearwater Bay, Kowloon, Hong Kong 999077, China.
  • Akkarasereenon K; Department of Chemistry, The Hong Kong University of Science and Technology, Clearwater Bay, Kowloon, Hong Kong 999077, China.
  • Liu L; Key Laboratory of Biopesticide and Chemical Biology (Ministry of Education), College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou 350002, China.
  • Lin R; College of Bee Science and Biomedicine, Fujian Agriculture and Forestry University, Fuzhou 350002, China.
  • Song L; Key Laboratory of Biopesticide and Chemical Biology (Ministry of Education), College of Plant Protection, Fujian Agriculture and Forestry University, Fuzhou 350002, China.
  • Tong R; Department of Chemistry, The Hong Kong University of Science and Technology, Clearwater Bay, Kowloon, Hong Kong 999077, China.
Org Lett ; 26(24): 5151-5156, 2024 Jun 21.
Article em En | MEDLINE | ID: mdl-38864512
ABSTRACT
We report a novel and environmentally friendly method for the ipso-bromination of arylboronic acids by exploiting the oxone/KBr system. We discovered that CuBr can catalyze the reaction and increase the yield from 63 to 97%. We believe that CuBr might catalyze the in situ generation of HOBr from oxone/KBr. The mild reaction condition permits tolerance of a diverse array of functional groups with exclusive regio- and chemoselectivity and allows low-cost large-scale reaction without explosion risk.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2024 Tipo de documento: Article País de afiliação: China