Transition-Metal-Catalyzed Direct C-H Alkenylation, Alkynylation, Benzylation, and Alkylation of (Hetero)arenes

被引:164
作者
Messaoudi, Samir [1 ]
Brion, Jean-Daniel [1 ]
Alami, Mouad [1 ]
机构
[1] Univ Paris 11, CNRS, BioCIS UMR 8076, Chim Therapeut Lab,Fac Pharm, F-92296 Chatenay Malabry, France
关键词
C-H activation; C-C coupling; Alkynes; Alkenylation; Alkynylation; Benzylation; Alkylation; Arenes; CROSS-COUPLING REACTION; MONOAMINE-OXIDASE-B; GACL3-CATALYZED ORTHO-ETHYNYLATION; INTERMOLECULAR DIRECT ARYLATION; PROTON-ABSTRACTION MECHANISM; SUZUKI-MIYAURA; BREAST-CANCER; IN-VITRO; DIHYDROFOLATE-REDUCTASE; AROMATASE INHIBITORS;
D O I
10.1002/ejoc.201000928
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Direct functionalization of (hetero) aromatic C-H bonds has recently emerged as a powerful tool for the functionalization of organic molecules. In the past decade, while many efforts have focused on the direct arylation of (hetero)arenes, much less attention has been devoted to the direct alkenylation, alkynylation, and benzylation of (hetero) arenes. This micro-review summarizes the development in this area to date, with the focus on how the substrate scope has been expanded through selection of more appropriate synthetic methods, such as the careful choice of catalysts, ligands, bases and reaction conditions.
引用
收藏
页码:6495 / 6516
页数:22
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