Recent Advances in Catalytic Enantioselective Fluorination Reactions

被引:250
|
作者
Lectard, Sylvain [1 ]
Hamashima, Yoshitaka [1 ,2 ]
Sodeoka, Mikiko [1 ]
机构
[1] RIKEN Adv Sci Inst, Wako, Saitama 3510198, Japan
[2] Univ Shizuoka, Sch Pharmaceut Sci, Suruga Ku, Shizuoka 4228526, Japan
关键词
asymmetric catalysis; electrophilic fluorination; fluorine chemistry; nucleophilic fluorination; organocatalysis; organometallic catalysis; CHIRAL PALLADIUM COMPLEXES; BETA-KETO-ESTERS; ASYMMETRIC ELECTROPHILIC FLUORINATION; ORGANOCATALYTIC ALPHA-FLUORINATION; CINCHONA ALKALOIDS F-CA-BF4; N-FLUOROAMMONIUM SALTS; CARBONYL-COMPOUNDS; BOND FORMATION; 1,3-DICARBONYL COMPOUNDS; BMS-204352 MAXIPOST(TM);
D O I
10.1002/adsc.201000624
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Since the incorporation of fluorine into biologically active compounds often enhances the properties of the parent compounds, there is a considerable demand for efficient enantioselective fluorination reactions. Over the past decade, a range of metal-catalyzed and organocatalyzed fluorination reactions has been developed. Nowadays, fluorine can be catalytically introduced into many compounds in good yield and with high enantioselectivity, and the scope of these reactions is broad. Herein, we review recent progress in the field of catalytic enantioselective fluorination reactions, including their scope and mechanism.
引用
收藏
页码:2708 / 2732
页数:25
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