2,2′-Bipyridine-3,3′-dicarboxylic carbohydrate esters and amides. Synthesis and preliminary evaluation as ligands in Cu(II)-catalysed enantioselective electrophilic fluorination

被引:21
作者
Assalit, Aurelie [1 ,2 ,3 ]
Billard, Thierry [1 ,2 ]
Chambert, Stephane [1 ,3 ]
Langlois, Bernard R. [1 ,2 ]
Queneau, Yves [1 ,3 ]
Coe, Diane [4 ]
机构
[1] Univ Lyon 1, CNRS, ICBMS, UMR5246,INSA Lyon,CPE Lyon, F-69622 Villeurbanne, France
[2] Univ Lyon 1, Lab SERCOF, Chevreul, France
[3] Inst Natl Sci Appl Lyon, Chim Organ Lab, Jules Verne, France
[4] GlaxoSmithKline, Resp CEDD, Med Res Ctr, Stevenage SG1 2NY, Herts, England
关键词
ORGANOCATALYTIC ALPHA-FLUORINATION; CINCHONA ALKALOIDS F-CA-BF4; N-FLUOROAMMONIUM SALTS; ASYMMETRIC CATALYSIS; MEDICINAL CHEMISTRY; BETA-KETOESTERS; BINDING-PROPERTIES; CRYSTAL-STRUCTURE; COMPLEXES; CYCLODEXTRIN;
D O I
10.1016/j.tetasy.2009.02.050
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A series of 10 new carbohydrate-substituted bipyridines were prepared from 2,2'-bipyridine-3,3'-dicarboxylic acid, itself easily available from ortho-phenanthroline. As a preliminary exploration of their use as chiral ligands, Cu(II)-catalysed asymmetric electrophilic fluorination of model beta-ketoesters using these simple and easily accessible chiral bipyridines was studied. Only modest enantioselectivity was observed in this reaction, although the ee was in a similar range as those provided by known and more elaborate ligands. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:593 / 601
页数:9
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