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DMSO-Promoted Difluoroalkylation of Organophosphonium Salts with Difluoroenol Silyl Ethers.

Zi-Lun YuJia-Wei ChenYu-Lan ChenRen-Jun ZhengMengtao MaJian-Ping ChenZhi-Liang ShenXue-Qiang Chu
Published in: Organic letters (2022)
An efficient method for the synthesis of β,β-di(hetero)aryl-α,α-difluorinated ketones using readily available organophosphonium salts and difluoroenol silyl ethers has been developed. This mild reaction features a good functional group tolerance, a scaled-up synthesis, and synthetic simplicity. By taking advantage of DMSO as a less-toxic promoter and solvent for the difluoroalkylation and C-P bond functionalization, the use of transition-metal catalysts and sensitive additives could be avoided.
Keyphrases
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  • gene expression
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  • highly efficient
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  • electron transfer