Palladium-catalyzed intermolecular α-arylation of N-protected 2-piperidinones

被引:59
作者
Cossy, J [1 ]
de Filippis, A [1 ]
Pardo, DG [1 ]
机构
[1] Ecole Super Phys & Chim Ind Ville Paris, CNRS, Chim Organ Lab, F-75231 Paris 05, France
关键词
D O I
10.1021/ol0350036
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
graphic The alpha-arylation of the zinc enolate of N-protected 2-piperidinones with aryl bromides in the presence of a palladium catalyst is described as a general method.
引用
收藏
页码:3037 / 3039
页数:3
相关论文
共 33 条
[1]  
BLAKE CH, 1997, J AM CHEM SOC, V119, P12382
[2]  
Bolm C, 2001, ANGEW CHEM INT EDIT, V40, P3285
[3]   BASE-CATALYZED HALOGEN DANCE, AND OTHER REACTIONS OF ARYL HALIDES [J].
BUNNETT, JF .
ACCOUNTS OF CHEMICAL RESEARCH, 1972, 5 (04) :139-&
[4]   AROMATIC NUCLEOPHILIC SUBSTITUTION REACTIONS [J].
BUNNETT, JF ;
ZAHLER, RE .
CHEMICAL REVIEWS, 1951, 49 (02) :273-412
[5]   Palladium-catalyzed α-arylation of carbonyl compounds and nitriles [J].
Culkin, DA ;
Hartwig, JF .
ACCOUNTS OF CHEMICAL RESEARCH, 2003, 36 (04) :234-245
[6]   C-C bond-forming reductive elimination of ketones, esters, and amides from isolated arylpalladium(II) enolates [J].
Culkin, DA ;
Hartwig, JF .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2001, 123 (24) :5816-5817
[7]  
Ehrentraut A, 2002, ADV SYNTH CATAL, V344, P209, DOI 10.1002/1615-4169(200202)344:2<209::AID-ADSC209>3.0.CO
[8]  
2-5
[9]   Highly active and selective catalysts for the formation of α-aryl ketones [J].
Fox, JM ;
Huang, XH ;
Chieffi, A ;
Buchwald, SL .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (07) :1360-1370
[10]  
Freund R, 2000, HELV CHIM ACTA, V83, P1247, DOI 10.1002/1522-2675(20000607)83:6<1247::AID-HLCA1247>3.0.CO