Department of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka 565-0871 (Japan) http://www.chem.eng.osaka-u.ac.jp/∼ogoshi-lab/en/index.html.
Angew Chem Int Ed Engl. 2016 Jan 4;55(1):341-4. doi: 10.1002/anie.201508266. Epub 2015 Oct 30.
A copper-catalyzed reaction of easily accessible α,α,α-trifluoromethylketones with various aldehydes affords difluoro-methylene compounds in the presence of diboron and NaOtBu. The key process of the reaction is the formation of a copper difluoroenolate by 1,2-addition of a borylcopper intermediate to α,α,α-trifluoromethylketones and subsequent β-fluoride elimination. Mechanistic studies including the isolation and characterization of a possible anionic copper alkoxide intermediate are also described.
一种铜催化的反应,使易得的α,α,α-三氟甲基酮与各种醛在二硼和 NaOtBu 的存在下反应,生成二氟亚甲基化合物。该反应的关键步骤是通过硼铜中间体对α,α,α-三氟甲基酮的 1,2-加成形成铜二氟烯醇盐,随后发生β-氟消除。也描述了包括可能的阴离子铜烷氧基金属中间体的分离和表征在内的机理研究。