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Toward C2-nitrogenated chromones by copper-catalyzed β-C(sp2)–H N-heteroarylation of enaminones
Organic Chemistry Frontiers ( IF 5.4 ) Pub Date : 2020-03-23 , DOI: 10.1039/d0qo00065e
Tian Luo 1, 2, 3, 4 , Jie-Ping Wan 1, 2, 3, 4 , Yunyun Liu 1, 2, 3, 4
Affiliation  

The unconventionally selective β-C(sp2)–H activation of enaminones in the presence of various nitrogen nucleophiles, including azoles and cyclic amines, leading to the synthesis of 2-nitrogenated chromones has been achieved by employing a catalytic system consisting of CuI, I2, PhI(OAc)2 and Na2CO3. The work discloses a new application of functonal enaminones in the synthesis of valuable heterocyclic scaffolds by switching the reaction pathway via unprecedented regioselectivity.

中文翻译:

铜催化的β-C(sp2)–H N-烯胺酮的杂芳基合成对C2-氮化的色酮

在多种氮亲核试剂(包括吡咯和环胺)的存在下,烯胺酮的非常规选择性β-C(sp 2)–H活化是通过使用由CuI组成的催化体系实现的,从而导致了2-氮代色酮的合成I 2,PhI(OAc)2和Na 2 CO 3。这项工作揭示了功能性烯胺酮在合成有价值的杂环骨架中的新应用,该合成是通过前所未有的区域选择性来切换反应途径而实现的。
更新日期:2020-03-23
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