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Organocatalysis in Inert C–H Bond Functionalization
Chemical Reviews ( IF 51.4 ) Pub Date : 2017-02-13 00:00:00 , DOI: 10.1021/acs.chemrev.6b00657
Yan Qin 1, 2 , Lihui Zhu 1, 2 , Sanzhong Luo 1, 2
Affiliation  

As two coexisting and fast-growing research fields in modern synthetic chemistry, the merging of organocatalysis and C–H bond functionalization is well foreseeable, and the joint force along this line has been demonstrated to be a powerful approach in making inert C–H bond functionalization more viable, predictable, and selective. In this review, we provide a comprehensive summary of organocatalysis in inert C–H bond functionalization over the past two decades. The review is arranged by types of inert C–H bonds including alkane C–H, arene C–H, and vinyl C–H as well as those activated benzylic C–H, allylic C–H, and C–H bonds alpha to the heteroatom such as nitrogen and oxygen. In each section, the discussion is classified by the explicit organocatalytic mode involved.

中文翻译:

惰性C–H键功能化中的有机催化

作为现代合成化学中两个并存且发展迅速的研究领域,有机催化与C-H键功能化的融合是可以预见的,并且沿着这一方向的联合力已被证明是制造惰性C-H键的有力方法。功能化更具可行性,可预测性和选择性。在这篇综述中,我们提供了过去20年中惰性C–H键功能化过程中有机催化的全面总结。综述按惰性CH键的类型排列,包括烷烃CH,芳烃CH和乙烯基CH以及活化的苄基CH,烯丙基CH和CH键与杂原子,例如氮和氧。在每个部分中,讨论都按照所涉及的显式有机催化模式进行分类。
更新日期:2017-02-13
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