A Route to α-Fluoroalkyl Sulfides from α-Fluorodiaroylmethanes

Autor: Wen-Bin Yi, Wan-zhao Shen, Guo-ping Lu, Ya-mei Lin
Rok vydání: 2016
Předmět:
Zdroj: Organic letters. 18(3)
ISSN: 1523-7052
Popis: α,α-Difluorodiaroylmethane can be used as a nucleophilic difluoromethylation reagent for generating α-thioaryl-α,α-difluoroacetophenones (Ar(1)COCF2SAr) and difluoromethylthiolated arenes (ArSCF2H) under transition-metal-free conditions. The reaction selectivity is mainly dependent on temperature. The method has also been extended to the synthesis of α-thioaryl-α-monofluoroacetophenones using α-monofluorodibenzoylmethane. Moreover, the benzoyl cation derived from α,α-difluorodibenzoylmethane can react with nucleophiles to afford the desired products in a one-pot process.
Databáze: OpenAIRE