Study on the mild, rapid and selective difluorocarbene-mediated triclassification of iododifluoroacetophenone with secondary amines and tree model for product classification
Reaction of Thiocarbonyl Fluoride Generated from Difluorocarbene with Amines
作者:Jiao Yu、Jin-Hong Lin、Ji-Chang Xiao
DOI:10.1002/anie.201710186
日期:2017.12.22
The reaction of thiocarbonyl fluoride, generated from difluorocarbene, with various amines under mild conditions is described. Secondary amines, primary amines, and o‐phenylenediamines are converted to thiocarbamoyl fluorides, isothiocyanates, and difluoromethylthiolated heterocycles, respectively. Thiocarbamoyl fluorides were further transformed into trifluoromethylated amines by using a one‐pot process
Efficient Docking–Migration Strategy for Selective Radical Difluoromethylation of Alkenes
作者:Jiajia Yu、Zhen Wu、Chen Zhu
DOI:10.1002/anie.201811346
日期:2018.12.21
Radical‐mediated difunctionalization of alkenes is a powerful tactic for olefin utilization. However, the transformation of unactivated alkenes still remains a formidable challenge. Now a conceptually new docking–migration strategy is presented for the difunctionalization of alkenes with photoredox catalysis. Both activated and unactivated alkenes are suitable substrates. A vast array of functional
[EN] DIFLUOROMETHYLATION OF UNSATURATED COMPOUNDS<br/>[FR] DIFLUOROMÉTHYLATION DE COMPOSÉS INSATURÉS
申请人:SCRIPPS RESEARCH INST
公开号:WO2013082028A1
公开(公告)日:2013-06-06
A reagent for carrying out a difluoromethylation reaction of unsaturated compounds and ring-nitrogen-containing aromatic compounds, a zinc difluoro-methanesulfinate, as well as a method for making the reagent and a method for its use are disclosed.
Difluoromethylation of Phenols and Thiophenols with the <i>S</i>-(Difluo-romethyl)sulfonium Salt: Reaction, Scope, and Mechanistic Study
作者:Guo-Kai Liu、Wen-Bing Qin、Xin Li、Li-Ting Lin、Henry N. C. Wong
DOI:10.1021/acs.joc.9b02424
日期:2019.12.20
A facile and practical approach for the difluoromethylation of phenols and thiophenols was described. Making use of the recently developed bench-stable S-(difluoromethyl)sulfonium salt as the difluorocarbene precursor, a wide variety of diversely functionalized phenols and thiophenols were readily converted to their corresponding aryl difluoromethyl ethers in good to excellent yields in the presence
A reagent for carrying out a difluoromethylation reaction of unsaturated compounds and ring-nitrogen-containing aromatic compounds, a zinc difluoro-methanesulfinate, as well as a method for making the reagent and a method for its use are disclosed.