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Rhodium-Catalyzed Regioselective C(sp2)−H Bond Activation Reactions of N-(Hetero)aryl-7-azaindoles and Cross-Coupling with α-Carbonyl Sulfoxonium Ylides
Tetrahedron Letters ( IF 1.5 ) Pub Date : 2020-01-11 , DOI: 10.1016/j.tetlet.2020.151627
Yan Tian , Xian-Qiang Kong , Jie Niu , Yi-Bo Huang , Zhao-Hua Wu , Bo Xu

We described a protocol for rhodium-catalyzed C(sp2)−H bond activation reactions of N-(hetero)aryl-7-azaindoles and cross-coupling with α-carbonyl sulfoxonium ylides. In the C−H activation reaction, the 7-azaindole moiety acts as a directing group, which results in high regioselectivity. The protocol features excellent chemical yields and good functional group tolerance.



中文翻译:

铑催化的N-(杂)芳基-7-氮杂吲哚的区域选择性C(sp 2)-H键活化反应以及与α-羰基ulf氧羰基盐的交叉偶联

我们描述了N-(杂)芳基-7-氮杂吲哚的铑催化的C(sp 2)-H键活化反应以及与α-羰基亚砜基鎓盐交叉偶联的方案。在CH活化反应中,7-氮杂吲哚部分作为导向基团,导致较高的区域选择性。该协议具有出色的化学收率和良好的官能团耐受性。

更新日期:2020-01-13
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