Phapale Vilas B, Cárdenas Diego J
Departamento de Química Orgánica, Universidad Autónoma de Madrid, Cantoblanco, Madrid 28049, Spain.
Chem Soc Rev. 2009 Jun;38(6):1598-607. doi: 10.1039/b805648j. Epub 2009 Mar 17.
The Negishi cross-coupling of organozinc reagents is a valuable tool for the formation of C-C bonds in the presence of functional groups. Although this reaction is catalysed by Ni or Pd complexes, the latter have been much more developed. Nevertheless, Ni derivatives have become important in recent years, especially for their activity in the formation of alkyl-alkyl bonds. The mechanisms involved in Ni-catalysed reactions are different from the usual catalytic cycle involving oxidative addition-transmetalation-reductive elimination that is generally accepted for Pd-catalysed reactions. This tutorial review presents the more recent advances in Ni-catalysed Negishi cross-couplings for the formation of different kinds of C-C bonds and discusses their proposed reaction mechanisms.
有机锌试剂的根岸交叉偶联反应是在官能团存在下形成碳-碳键的一种重要工具。尽管该反应由镍或钯配合物催化,但后者的发展更为成熟。然而,近年来镍衍生物变得很重要,特别是因其在形成烷基-烷基键方面的活性。镍催化反应所涉及的机理不同于钯催化反应通常所接受的氧化加成-金属转移-还原消除的催化循环。本教程综述介绍了镍催化根岸交叉偶联反应在形成不同类型碳-碳键方面的最新进展,并讨论了其提出的反应机理。