化学
废止
马来酰亚胺
吲唑
区域选择性
组合化学
金属化
选择性
催化作用
立体化学
有机化学
分子内力
作者
Chenhao Guo,Bin Li,Huilai Liu,Xiaopeng Zhang,Xinying Zhang,Xuesen Fan,Xinying Zhang,Xuesen Fan
出处
期刊:Organic Letters
[American Chemical Society]
日期:2019-09-04
卷期号:21 (18): 7189-7193
被引量:121
标识
DOI:10.1021/acs.orglett.9b01889
摘要
A dehydrogenative annulation of 2-arylindazoles with maleimides for the switchable synthesis of indazolo[2,3-a]pyrrolo[3,4-c]quinolinones or spiroindolo[1,2-b]indazole-11,3′-pyrrolidinones is presented. Mechanistically, the formation of the title compounds involves a Rh(III)-catalyzed C–H metalation of 2-arylindazole, followed by maleimide insertion and intramolecular cyclization. Interestingly, the selectivity to form the fused or spiro compounds could be switched by resorting to different additives. The notable features of this protocol include simple substrates and excellent atom economy and regioselectivity.
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