Recent advances using [Cp*Co(CO)I2] catalysts as a powerful tool for C-H functionalisation

被引:112
作者
Chirila, Paula G.
Whiteoak, Christopher J. [1 ]
机构
[1] Sheffield Hallam Univ, Biomol Sci Res Ctr BMRC, Fac Hlth & Wellbeing, City Campus,Howard St, Sheffield S1 1WB, S Yorkshire, England
关键词
REDOX-NEUTRAL SYNTHESIS; PAUSON-KHAND REACTION; N BOND FORMATION; COBALT(III)-CATALYZED SYNTHESIS; INDOLE SYNTHESIS; EFFICIENT SYNTHESIS; TERMINAL ALKYNES; ACTIVATION; ANNULATION; AMIDATION;
D O I
10.1039/c7dt01980g
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Expansion of the synthetic chemists' toolbox is currently a topic of great interest, with successes providing access to novel compounds and more efficient routes towards new and known pharmaceuticals and agrochemicals. In this context, the development and application of first-row transition metal-catalysed C-H functionalisation protocols is seen as a key opportunity. This perspective provides a brief background of the discovery and application of high-valent cobalt-catalysis in C-H functionalisation, before detailing examples of recent advances in this field using the powerful [Cp*Co(CO)I-2] catalysts for both terminal couplings and heterocycle formation. Finally, a discussion on the detection and isolation of elusive reactive intermediates in high-valent cobalt-catalysed C-H functionalisation, shedding light on how these catalyst systems operate, will be provided.
引用
收藏
页码:9721 / 9739
页数:19
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