| Literature DB >> 25196839 |
Zhiyu Jia1, Erik Gálvez, Rosa María Sebastián, Roser Pleixats, Ángel Álvarez-Larena, Eddy Martin, Adelina Vallribera, Alexandr Shafir.
Abstract
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.Entities:
Keywords: CH functionalization; dehydrogenative CC coupling; hypervalent iodine; iodonium-Claisen rearrangement; α-arylation
Year: 2014 PMID: 25196839 DOI: 10.1002/anie.201405982
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336