4.5 Article

A visible-light-induced, metal-free bis-arylation of 2,5-dichlorobenzoquinone

期刊

BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY
卷 17, 期 -, 页码 2315-2320

出版社

BEILSTEIN-INSTITUT
DOI: 10.3762/bjoc.17.149

关键词

benzoquinone; diazonium salts; Green Chemistry; Meerwein arylation; photoredox

资金

  1. KU Leuven [C14/19/78]
  2. FWO-Vlaanderen [G0F6619N]
  3. Hercules Foundation of the Flemish Government [20100225-7]

向作者/读者索取更多资源

A metal-free protocol for the direct bis-arylation of 2,5-dichlorobenzoquinone with aryldiazonium salts is reported in this study. The reactive salts are generated in situ and converted to radicals through irradiation with visible light. Furthermore, reaction products precipitate from the solvent, eliminating the need for purification and providing a novel green method for the synthesis of versatile bis-electrophiles.
A metal-free protocol for the direct bis-arylation of 2,5-dichlorobenzoquinone with aryldiazonium salts is reported. The reactive salts are generated in situ and converted to radicals through irradiation with visible light. Reaction products precipitate from the solvent, eliminating the need for purification and thus providing a novel green method for the synthesis of versatile bis-electrophiles.

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