Regio- and stereoselective synthesis of vicinal fluorohydrins

被引:54
|
作者
Haufe, G [1 ]
机构
[1] Univ Munster, Inst Organ Chem, D-48149 Munster, Germany
关键词
condensation; enzyme-catalysis; epoxides; fluorohydrins; fluoroketones; hydrofluorination; reduction; resolution; ring opening; stereoselectivity; synthesis;
D O I
10.1016/j.jfluchem.2004.01.023
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Vicinal fluorohydrins are useful building blocks as well as important targets for synthesis of bioactive compounds or new materials. This review gives an overview on regio- and stereoselective, particularly enantioselective, syntheses of such compounds by building block methods, reduction of alpha-fluoro carbonyl compounds and ring opening of epoxides with hydrofluorinating reagents. Resolution of racemic vicinal fluorohydrins using enzyme-catalyzed reactions will also be discussed in detail. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:875 / 894
页数:20
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