4.7 Article

Synthesis of Fluorinated β-Ketosulfones and gem-Disulfones by Nucleophilic Fluoroalkylation of Esters and Sulfinates with Di- and Monofluoromethyl Sulfones

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 74, Issue 10, Pages 3767-3771

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo900320b

Keywords

-

Funding

  1. National Natural Science Foundation of China [20502029, 20772144, 20825209, 20832008]
  2. Chinese Academy of Sciences

Ask authors/readers for more resources

An efficient and practically useful method for the preparation of alpha-functionalized mono- and difluoro(phenylsulfonyl)methanes by using a nucleophilic fluoroalkylation methodology was developed. alpha,alpha-Difluoro-P-ketosulfones, alpha-monofluoro-beta-ketosulfones, and alpha-fluoro disulfones were successfully prepared in excellent yields by nucleophilic fluoroalkylation of esters and sulfinates with PhSO2CF2H and PhSO2CH2F reagents.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available