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Sterically Controlled Cu-Catalyzed or Transition-Metal-Free Cross-Coupling of gem-Difluoroalkenes with Tertiary, Secondary, and Primary Alkyl Grignard Reagents

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Figshare2016-08-29 更新2026-04-29 收录
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https://figshare.com/articles/dataset/Sterically_Controlled_Cu-Catalyzed_or_Transition-Metal-Free_Cross-Coupling_of_i_gem_i_-Difluoroalkenes_with_Tertiary_Secondary_and_Primary_Alkyl_Grignard_Reagents/3661350
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A robust copper-catalyzed or transition-metal-free cross-coupling of gem-difluoroalkenes with tertiary, secondary, and primary alkyl Grignard reagents has been developed. Remarkably, the tertiary and secondary alkylation of gem-difluoroalkenes proceeded very smoothly in the presence of 25 mol % of CuCN or under transition-metal-free conditions, affording the tertiary and secondary alkyl-substituted fluoroalkenes in good to excellent yields with excellent Z stereoselectivity.
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2016-08-29
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