The Cross-Dehydrogenative Coupling of Csp3-H Bonds: A Versatile Strategy for C-C Bond Formations

被引:1728
作者
Girard, Simon A. [1 ,2 ]
Knauber, Thomas [1 ,2 ]
Li, Chao-Jun [1 ,2 ]
机构
[1] McGill Univ, Dept Chem, Montreal, PQ H3A 0B8, Canada
[2] McGill Univ, FQRNT Ctr Green Chem & Catalysis, Montreal, PQ H3A 0B8, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
CC coupling; C-H activation; cross-coupling; green chemistry; synthetic methods; CATALYZED OXIDATIVE ARYLALKYLATION; FREE-RADICAL REACTIONS; ALDEHYDE-ALKYNE-AMINE; MANNICH-TYPE REACTION; CYCLIC BENZYL ETHERS; CARBON-CARBON BONDS; H BOND; TRANSITION-METAL; TERTIARY-AMINES; NUCLEOPHILIC CHARACTER;
D O I
10.1002/anie.201304268
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Over the last decade, substantial research has led to the introduction of an impressive number of efficient procedures which allow the selective construction of CC bonds by directly connecting two different CH bonds under oxidative conditions. Common to these methodologies is the generation of the reactive intermediates in situ by activation of both CH bonds. This strategy was introduced by the group of Li as cross-dehydrogenative coupling (CDC) and discloses waste-minimized synthetic alternatives to classic coupling procedures which rely on the use of prefunctionalized starting materials. This Review highlights the recent progress in the field of cross-dehydrogenative Csp3C formations and provides a comprehensive overview on existing procedures and employed methodologies.
引用
收藏
页码:74 / 100
页数:27
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