Catalytic Dehydrogenative Cross-Coupling: Forming Carbon-Carbon Bonds by Oxidizing Two Carbon-Hydrogen Bonds

被引:3507
作者
Yeung, Charles S. [1 ]
Dong, Vy M. [1 ]
机构
[1] Univ Toronto, Dept Chem, Toronto, ON M5S 3H6, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大创新基金会;
关键词
C-H BOND; BAYLIS-HILLMAN REACTION; ELECTRON-DEFICIENT POLYFLUOROARENES; INTRAMOLECULAR OXIDATIVE ALKYLATION; HOMOGENEOUS PALLADIUM(II) COMPOUNDS; METALATION-DEPROTONATION MECHANISM; ENANTIOSELECTIVE TOTAL-SYNTHESIS; HYPERVALENT IODINE(III) REAGENT; VISIBLE-LIGHT PHOTOCATALYSIS; INHIBITOR CARBAZOQUINOCIN-C;
D O I
10.1021/cr100280d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transformations that can be categorized as catalytic dehydrogenative cross-couplings are reviewed providing handy reference for chemists interested in using catalytic dehydrogenative coupling in multistep synthesis and those interested in inventing greener methods for C-C bond construction. In 2002, the groups of de Vries and van Leeuwen reported an exceptionally mild oxidative Heck-type olefination that uses amide directing groups to control reactivity and regioselectivity. The Yu lab reported Pd-catalyzed olefination of electron-deficient arenes that occurs with meta-selectivity and envisioned a novel ligand Pyr with steric encumbrance at the exterior of the ligand. the groups of Hu and You demonstrated that other classes of nitrogen-containing heterocycles undergo facile and regioselective arylation with stoichiometric amounts of Cu(OAc)2.
引用
收藏
页码:1215 / 1292
页数:78
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