Cross-couplings of unactivated secondary alkyl halides: Room-temperature nickel-catalyzed Negishi reactions of alkyl bromides and iodides

被引:287
作者
Zhou, JR [1 ]
Fu, GC [1 ]
机构
[1] MIT, Dept Chem, Cambridge, MA 02139 USA
关键词
D O I
10.1021/ja0389366
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of a nickel- or palladium-catalyzed method for cross-coupling unactivated secondary alkyl halides has been a long-standing challenge in synthetic chemistry. This communication describes a simple catalyst system-Ni(cod)2/s-Bu-Pybox-that achieves room-temperature Negishi reactions of an array of functionalized primary and secondary alkyl bromides and iodides. Copyright © 2003 American Chemical Society.
引用
收藏
页码:14726 / 14727
页数:2
相关论文
共 29 条
[1]  
Boudier A, 2000, ANGEW CHEM INT EDIT, V39, P4414, DOI 10.1002/1521-3773(20001215)39:24<4414::AID-ANIE4414>3.0.CO
[2]  
2-C
[3]   Advances in functional-group-tolerant metal-catalyzed alkyl-alkyl cross-coupling reactions [J].
Cárdenas, DJ .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (04) :384-387
[4]  
Cárdenas DJ, 1999, ANGEW CHEM INT EDIT, V38, P3018, DOI 10.1002/(SICI)1521-3773(19991018)38:20<3018::AID-ANIE3018>3.0.CO
[5]  
2-F
[6]  
Devasagayaraj A, 1995, ANGEW CHEM INT EDIT, V34, P2723
[7]  
Diederich F., 1998, METAL CATALYZED CROS, DOI DOI 10.1002/9783527612222
[8]  
Erdik E, 1996, ORGANOZINC REAGENTS
[9]  
Giovannini R, 1998, ANGEW CHEM INT EDIT, V37, P2387, DOI 10.1002/(SICI)1521-3773(19980918)37:17<2387::AID-ANIE2387>3.0.CO
[10]  
2-M