Nickel complexes for catalytic C-H bond functionalization

被引:37
作者
Johnson, S. A. [1 ]
机构
[1] Univ Windsor, Dept Chem & Biochem, Windsor, ON N9B 3P4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
CARBON-CARBON BONDS; DIRECT ALKYLATION; OXIDATIVE ADDITION; DIRECT ARYLATION; ORGANOMETALLIC CHEMISTRY; FLUORINATED AROMATICS; C(SP(3))-H BONDS; SN BONDS; ACTIVATION; HYDROGEN;
D O I
10.1039/c5dt00032g
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The direct catalytic functionalization of traditionally unreactive C-H bonds is an atom-economic transformation that has become increasingly important and commonplace in synthetic applications. In general, 2nd and 3rd row transition metal complexes are used as catalysts in these reactions, whereas the less costly and more abundant 1st row metal complexes have limited utility. This Perspective article summarizes progress from our laboratory towards understanding the fundamental issues that complicate the use of Ni complexes for catalytic C-H bond functionalization, as well as approaches to overcoming these limitations. In practice it is found that Ni complexes can functionalize C-H bonds by processes that, to date, have not been observed with the heavier metals. An example is provided by the catalytic stannylation of C-H bonds with tributylvinyltin, Bu3SnCH=CH2, which produces ethylene as a by-product.
引用
收藏
页码:10905 / 10913
页数:9
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