Pd-catalyzed cross-coupling reactions of alkyl halides

被引:428
作者
Kambe, Nobuaki [1 ]
Iwasaki, Takanori [1 ]
Terao, Jun [2 ]
机构
[1] Osaka Univ, Grad Sch Engn, Dept Appl Chem, Suita, Osaka 5650871, Japan
[2] Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan
关键词
SUZUKI-MIYAURA COUPLINGS; POSSESS BETA-HYDROGENS; ARYL GRIGNARD-REAGENTS; CARBON BOND FORMATION; ROOM-TEMPERATURE; OXIDATIVE-ADDITION; ORGANOMETALLIC COMPOUNDS; ARYLBORONIC ACIDS; BENZYL HALIDES; RELATIVE REACTIVITIES;
D O I
10.1039/c1cs15129k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cross-coupling reactions have become indispensable tools for creating carbon-carbon (or heteroatom) bonds in organic synthesis. Like in other important transition metal catalyzed reactions, such as metathesis, addition, and polymerization, unsaturated compounds are usually employed as substrates for cross-coupling reactions. However during the past decade, a great deal of effort has been devoted to the use of alkyl halides as saturated compounds in cross-coupling reactions, which has resulted in significant progress in this undeveloped area by introducing new effective ligands. Many useful catalytic systems are now available for synthetic transformations based on C(sp)3-C(sp)3, C-sp3-C(sp)2 and C-sp3-C-sp bond formation as complementary methods to conventional C(sp)2-C(sp)2, C(sp)2-C-sp and C-sp-C-sp coupling. This tutorial review summarizes recent advances in cross-coupling reactions of alkyl halides and pseudohalides catalyzed by a palladium complex.
引用
收藏
页码:4937 / 4947
页数:11
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