Department of Chemistry and Centro de Innovación en Química Avanzada (ORFEO-CINQA), Universitat Autònoma de Barcelona, Bellaterra (Spain).
Angew Chem Int Ed Engl. 2014 Oct 13;53(42):11298-301. doi: 10.1002/anie.201405982. Epub 2014 Sep 4.
The α-arylation of carbonyl compounds is generally accomplished under basic conditions, both under metal catalysis and via aryl transfer from the diaryl λ(3)-iodanes. Here, we describe an alternative metal-free α-arylation using ArI(O2CCF3)2 as the source of a 2-iodoaryl group. The reaction is applicable to activated ketones, such as α-cyanoketones, and works with substituted aryliodanes. This formal C-H functionalization reaction is thought to proceed through a [3,3] rearrangement of an iodonium enolate. The final α-(2-iodoaryl)ketones are versatile synthetic building blocks.
羰基化合物的α-芳基化反应通常在碱性条件下进行,无论是在金属催化下还是通过二芳基λ(3)-碘烷的芳基转移。在这里,我们描述了一种使用 ArI(O2CCF3)2 作为 2-碘芳基源的无金属的替代α-芳基化方法。该反应适用于活化的酮,如α-氰基酮,并且可以与取代的芳基碘烷反应。这种形式的 C-H 官能化反应被认为是通过碘翁盐的[3,3]重排来进行的。最终的α-(2-碘芳基)酮是多功能的合成砌块。