122590-94-7Relevant articles and documents
Nucleophilic fluoroalkylation of epoxides with fluorinated sulfones
Ni, Chuanfa,Li, Ya,Hu, Jinbo
, p. 6829 - 6833 (2006)
The unprecedented nucleophilic fluoroalkylation of simple epoxides with fluorinated sulfones was achieved to give the β-fluoroalkyl alcohols in one step. The negative "fluorine effect" in the nucleophilic fluoroalkylation of epoxides with fluorinated carbanions was probed by the reactivity comparison between carbanions PhSO2CF2 - (3) and PhSO2CCl2- (4) and between carbanions PhSO2CHF- (7) and PhSO2CHCl - (13). The mediation of this fluorine effect by introducing another electron-withdrawing benzenesulfonyl group was found to be an effective way to significantly increase the nucleophilicity of the fluorinated carbanions, with the reactivity order [(PhSO2)2CF-] (16) > PhSO2CFH- (7) ? PhSO2CF2 - (3).
Mono and difluorination of centers α to sulfonates and phosphonates using AcOF
Vints, Inna,Gatenyo, Julia,Rozen, Shlomo
, p. 66 - 69 (2013/03/29)
Acetyl hypofluorite, made easily from diluted fluorine and AcONa is very efficient in fluorinating anionic centers. Compounds containing the moieties CH2SO2 or COCH2PO react with bases to create the corresponding anions wh