Recent Advances in Difluoromethylation Reaction

被引:114
作者
Lu, Yang [1 ]
Liu, Chao [1 ]
Chen, Qing-Yun [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Organ Chem, Key Lab Organofluorine Chem, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
Direct difluoromethylation; stepwise difluoromethylation; difluoromethyl synthons; fluorinating reagent; difluorocarbene; ALPHA; BETA-UNSATURATED CARBOXYLIC-ACIDS; COPPER-MEDIATED DIFLUOROMETHYLATION; RUPPERT-PRAKASH REAGENT; ARYL BORONIC ACIDS; CARBONYL-COMPOUNDS; NUCLEOPHILIC DIFLUOROMETHYLATION; OXIDATIVE ACTIVATION; UNACTIVATED ALKENES; N-ARYLACRYLAMIDES; DIFLUOROCARBENE;
D O I
10.2174/1385272819666150615235605
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Impressive progress has been achieved during the past decade in the incorporation of various fluroine-containing groups, especially lightly fluorinated groups, into organic compounds. Among them, the introduction of difluoromethyl group into a compound commonly brings about many special and important effects. Two major strategies have been developed: (1) direct transfer of a CF2H group into target molecules (direct difluoromethylation); (2) the introduction of a functionlized moiety into organic substrates followed by subsequent transformation of the functional group into hydrogen or fluorine atoms (stepwise difluoromethylation). This mini review summarizes the recent developments in the selective direct and stepwise difluoromethyaltion methods during the past six years.
引用
收藏
页码:1638 / 1650
页数:13
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