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C(sp3)-H dehydrogenation and C(sp2)-H alkoxy carbonylation of inactivated cyclic amines towards functionalized N-heterocycles
Chemical Communications ( IF 4.9 ) Pub Date : 2017-03-20 00:00:00 , DOI: 10.1039/c6cc10227a
Yan He 1, 2, 3, 4, 5 , Fang Wang 1, 2, 3, 4, 5 , Xinying Zhang 1, 2, 3, 4, 5 , Xuesen Fan 1, 2, 3, 4, 5
Affiliation  

A novel and efficient synthesis of tetrahydropyridine-, dihydropyrrole-, and tetrahydroazepine-3-carboxylates via cascade reactions of cyclic amines with CO and alcohols is presented. To our knowledge, this should be the first example in which functionalized N-heterocycles were prepared through Pd-catalyzed C(sp3)-H dehydrogenation and C(sp2)-H carbonylation of cyclic amines.

中文翻译:

灭活的环胺向官能化的N-杂环的C(sp3)-H脱氢和C(sp2)-H烷氧基羰基化

通过环胺与CO和醇的级联反应,提出了一种新颖而有效的四氢吡啶-,二氢吡咯-和四氢氮杂-3-羧酸酯的合成方法。据我们所知,这应该是第一个通过钯催化环胺的C(sp 3)-H脱氢和C(sp 2)-H羰基化制备N杂环的例子。
更新日期:2017-04-06
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