Copper-Catalyzed N-H/C-H Sequential Relay Oxidative Radical Carboannulation: Construction of Diversely Substituted [60]Fullerene-Fused Tetrahydrocyclopenta[b]indoles

被引:18
作者
Liu, Tong-Xin [1 ]
Wei, Juan [1 ]
Zhang, Pengling [1 ]
Ru, Yifei [1 ]
Ma, Jinliang [1 ]
Zhang, Xingjie [1 ]
Ma, Nana [1 ]
Zhang, Guisheng [1 ]
机构
[1] Henan Normal Univ, Collaborat Innovat Ctr Henan Prov Green Mfg Fine, Henan Key Lab Organ Funct Mol & Drug Innovat, Key Lab Green Chem Media & React,Minist Educ,Sch, Xinxiang 453007, Henan, Peoples R China
关键词
TRANSITION-METAL-FREE; 1,3-DIPOLAR CYCLOADDITION; FULLERENE CHEMISTRY; ONE-POT; DERIVATIVES; ANNULATION; C-60; FUNCTIONALIZATION; HETEROANNULATION; HYDROFULLERENES;
D O I
10.1021/acs.orglett.9b02354
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Reported herein is a new copper-catalyzed N-H/C-H sequential relay oxidative radical carboannulation of [60]fullerene with C2-functionalized free indoles for the direct construction of novel [60]fullerene-fused tetrahydrocyclopenta[b]indoles. The transformation shows high regioselectivity and atom economy, broad substrate scope, and good functional group tolerance, providing an efficient and practical approach to access diversely substituted fullerene-fused polycyclic derivatives from simple hydrocarbons.
引用
收藏
页码:6461 / 6465
页数:5
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