期刊
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2018, 期 44, 页码 6068-6082出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201800299
关键词
Synthetic methods; C-C bond formation; Cross-coupling; Direct arylation; C-H activation
资金
- Science Foundation Ireland [SFI/12/IP/1315]
- Synthesis and Solid State Pharmaceutical Centre (SSPC) [SFI/12/RC/2275]
- European Cooperation in Science and Technology (COST) initiative [CA15106]
C-H activation has emerged as a viable alternative to traditional C-C bond forming reactions such as the Suzuki-Miyaura, Stille, Negishi and others. However, C-H activation is rarely employed in total synthesis or fine chemical manufacture, particularly as an end-game strategy. This may be due to the harsh conditions typically required. For C-H activation to become a truly useful and versatile methodology, conditions must emerge which are applicable to compounds with multiple functionalities. In this review, we hope to inspire the chemistry community to focus their efforts on milder conditions for C-H activation and cross-dehydrogenative coupling. To this end, we have focused on describing C-H activation as it has been applied to several classes of biologically interesting, but chemically sensitive motifs: the 2-pyrones, 2-pyridones, 2-coumarins and 2-quinolones.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据