Cobalt-Catalyzed C(sp3)-H Functionalization Reactions

被引:81
作者
Yoshino, Tatsuhiko [1 ]
Matsunaga, Shigeki [1 ]
机构
[1] Hokkaido Univ, Fac Pharmaceut Sci, Kita Ku, Kita 12 Nishi 6, Sapporo, Hokkaido 0600812, Japan
关键词
C-H activation; cobalt; directing groups; homogeneous catalysis; synthetic methods; C-H BONDS; CARBON-CARBON; AMIDO TRANSFER; ACTIVATION; AMIDATION; HYDROGEN; CARBONYLATION; ALKYNES; HYDROARYLATION; CYCLIZATION;
D O I
10.1002/ajoc.201800195
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
C-H functionalization reactions hold great potential for the streamlined synthesis of complex molecules and are currently a hot topic in organic synthesis. Among the various transition metals that have been used, cobalt has recently attracted increased attention as a catalyst for C-H functionalization reactions, owing to its ready availability and high reactivity. Although a number of cobalt-catalyzed C(sp(2))-H functionalization reactions have been reported to date, C(sp(3))-H functionalization reactions remain challenging. This Focus Review summarizes recent progress in cobalt-catalyzed C(sp(3))-H functionalization reactions that involve C-H activation to form organometallic intermediates.
引用
收藏
页码:1193 / 1205
页数:13
相关论文
共 88 条
[1]   Carboxylate-Assisted Transition-Metal-Catalyzed C-H Bond Functionalizations: Mechanism and Scope [J].
Ackermann, Lutz .
CHEMICAL REVIEWS, 2011, 111 (03) :1315-1345
[2]   A warning on the use of radical traps as a test for radical mechanisms:: They react with palladium hydrido complexes [J].
Albéniz, AC ;
Espinet, P ;
López-Fernández, R ;
Sen, A .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (38) :11278-11279
[3]  
Ammann S.E., 2016, Angew. Chem. Int. Ed, V128, P9723
[4]   Enantioselective Allylic C-H Oxidation of Terminal Olefins to Isochromans by Palladium(II)/Chiral Sulfoxide Catalysis [J].
Ammann, Stephen E. ;
Liu, Wei ;
White, M. Christina .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2016, 55 (33) :9571-9575
[5]  
[Anonymous], 2017, ANGEW CHEM, V129, P16777
[6]  
[Anonymous], 2012, ANGEW CHEM, DOI DOI 10.1002/ANIE.201201666
[7]  
[Anonymous], 2018, ANGEW CHEM, V130, P4309
[8]  
[Anonymous], 2013, ANGEW CHEM-GER EDIT
[9]  
[Anonymous], 2016, ANGEW CHEM
[10]  
Arockiam PB, 2012, CHEM REV, V112, P5879, DOI [10.1021/cr300153J, 10.1021/cr300153j]