Recent advances in cobalt-catalyzed allylic functionalization

被引:32
|
作者
Han, Jun-Fa [1 ]
Guo, Peng [1 ]
Zhang, Xiang-Gui [1 ]
Liao, Jia-Bin [1 ]
Ye, Ke-Yin [1 ]
机构
[1] Fuzhou Univ, Fujian Prov Univ, Coll Chem, Key Lab Mol Synth & Funct Discovery, Fuzhou 350108, Peoples R China
基金
中国国家自然科学基金;
关键词
PAUSON-KHAND REACTION; C-H ALLYLATION; CARBONYL-COMPOUNDS; ALKYL-HALIDES; HECK REACTION; COBALT(III)-CATALYZED ALLYLATION; ENANTIOSELECTIVE ALLYLATION; CYCLOADDITION REACTIONS; ASYMMETRIC ALLYLATION; COUPLING REACTION;
D O I
10.1039/d0ob01581d
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Unlike many other state-of-the-art transition-metal-catalyzed allylic substitutions, cobalt-catalyzed allylic substitution has received much less attention from synthetic chemists for a long time despite the fact that cobalt is an earth-abundant, low-cost and thus much more sustainable option as either a reagent or a catalyst in organic synthesis. Recently, there has been an upsurge in the use of cobalt catalysis in allylic functionalization reactions, including allylic substitution, nucleophilic allylation, and Heck-type allylic functionalization, to construct synthetically significant building blocks featuring a double bond available for diverse downstream synthetic manipulations. This review highlights the current development of cobalt catalysis in allylic functionalization with an in-depth discussion of the reaction scope and mechanistic insights.
引用
收藏
页码:7740 / 7750
页数:11
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