Palladium-catalyzed homocoupling reactions between two Csp3-Csp3 centers

被引:43
作者
Lei, AW [1 ]
Zhang, XM [1 ]
机构
[1] Penn State Univ, Davey Lab 152, Dept Chem, University Pk, PA 16802 USA
关键词
D O I
10.1021/ol0258536
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
[GRAPHICS] A novel palladium-catalyzed coupling reaction between two Csp(3)-Csp(3) centers has been investigated. This protocol is initiated by the oxidative addition of an alpha-halo carbonyl compound to a palladium(0) species, followed by the double transmetalation. The key dialkyl palladium intermediate undergoes reductive elimination to form the desired coupling product.
引用
收藏
页码:2285 / 2288
页数:4
相关论文
共 32 条
[1]  
[Anonymous], 1998, TRANSITION METALS OR
[2]  
Cárdenas DJ, 1999, ANGEW CHEM INT EDIT, V38, P3018, DOI 10.1002/(SICI)1521-3773(19991018)38:20<3018::AID-ANIE3018>3.0.CO
[3]  
2-F
[4]  
Chemler SR, 2001, ANGEW CHEM INT EDIT, V40, P4544, DOI 10.1002/1521-3773(20011217)40:24<4544::AID-ANIE4544>3.0.CO
[5]  
2-N
[6]  
Collman J.P., 1987, PRINCIPLES APPL ORGA
[7]  
CORNILS B, 1999, APPL HOMOGENEOUS CAT
[8]   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
[9]  
Devasagayaraj A, 1995, ANGEW CHEM INT EDIT, V34, P2723
[10]  
DEVASAGAYARAJ A, 1995, ANGEW CHEM, V107, P2952