Transition-Metal-Catalyzed Laboratory-Scale Carbon-Carbon Bond-Forming Reactions of Ethylene

被引:88
|
作者
Saini, Vaneet [1 ]
Stokes, Benjamin J. [1 ]
Sigman, Matthew S. [1 ]
机构
[1] Univ Utah, Dept Chem, Salt Lake City, UT 84112 USA
基金
美国国家卫生研究院;
关键词
C-C coupling; ethylene; fine chemicals; homogeneous catalysis; synthetic methods; C-H BOND; RING-CLOSING METATHESIS; ELECTROPHILIC DISPLACEMENT REACTIONS; ALKYNE CROSS-METATHESIS; ASYMMETRIC HYDROVINYLATION; HECK REACTION; ENANTIOSELECTIVE HYDROVINYLATION; 1,3-DIENE SYNTHESIS; SELECTIVE HYDROVINYLATION; REGIOSELECTIVE ACYLATION;
D O I
10.1002/anie.201303916
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ethylene, the simplest alkene, is the most abundantly synthesized organic molecule by volume. It is readily incorporated into transition-metal-catalyzed carbon-carbon bond-forming reactions through migratory insertions into alkylmetal intermediates. Because of its D-2h symmetry, only one insertion outcome is possible. This limits byproduct formation and greatly simplifies analysis. As described within this Minireview, many carbon-carbon bond-forming reactions incorporate a molecule (or more) of ethylene at ambient pressure and temperature. In many cases, a useful substituted alkene is incorporated into the product.
引用
收藏
页码:11206 / 11220
页数:15
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