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钯催化的卤代烷烃交叉偶联反应。

Pd-catalyzed cross-coupling reactions of alkyl halides.

机构信息

Department of Applied Chemistry, Graduate School of Engineering, Osaka University, Suita, Osaka 565-0871, Japan.

出版信息

Chem Soc Rev. 2011 Oct;40(10):4937-47. doi: 10.1039/c1cs15129k. Epub 2011 Jul 25.

Abstract

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(sp(3))-C(sp(2)) and C(sp(3))-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.

摘要

交叉偶联反应已成为有机合成中构建碳-碳(或杂原子)键的不可或缺的工具。与其他重要的过渡金属催化反应(如复分解、加成和聚合)一样,不饱和化合物通常被用作交叉偶联反应的底物。然而,在过去的十年中,人们致力于将卤代烷烃作为饱和化合物用于交叉偶联反应,通过引入新的有效配体,这一未开发领域取得了重大进展。许多有用的催化体系现在可用于基于 C(sp(3))-C(sp(3))、C(sp(3))-C(sp(2)) 和 C(sp(3))-C(sp)键形成的合成转化,作为对传统 C(sp(2))-C(sp(2))、C(sp(2))-C(sp) 和 C(sp)-C(sp)偶联的补充方法。本综述总结了钯配合物催化的卤代烷和拟卤代物交叉偶联反应的最新进展。

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