Green Light Triggered Radical Annulation for the Synthesis of Indenone by Metal-Free Photocatalysis

被引:2
作者
He, Xing [1 ]
Ji, Jia-Qi [1 ]
Zhao, Meng-Yan [1 ]
Ma, Chun-Hua [1 ]
Zhang, Dan-Dan [1 ]
Xu, Gui-Qing [1 ]
Ding, Qing-Jie [1 ]
Cui, Zhen-Wei [2 ]
Jiang, Yu-Qin [1 ]
机构
[1] Henan Normal Univ, Collaborat Innovat Ctr Henan Prov Green Mfg Fine C, Henan Engn Res Ctr Chiral Hydroxyl Pharmaceut, Sch Chem & Chem Engn,Minist Educ,Key Lab Green Che, Xinxiang 453007, Peoples R China
[2] Chongqing Aoshe Biol Chem Co LTD, Chongqing 400712, Peoples R China
关键词
Photocatalysis; Indenone; Rhodamine; 6G; Metal-free; Radical; CARBONYLATIVE CYCLIZATION REACTIONS; AEROBIC PHOTOOXIDATIVE CLEAVAGE; MEOTF-INDUCED CARBOANNULATION; ALPHA-KETO ACIDS; C-H BOND; CATALYZED ANNULATION; PHOTOREDOX CATALYSIS; CARBOXYLIC-ACIDS; ALKYNES; GENERATION;
D O I
10.1002/ejoc.202400579
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Low-energy light, endowing with excellent characteristics of lower energy, fewer side reactions, more abundance in solar light. The scenario has been developed for the fabrication of indenone through a low-energy green light driven radical annulation reaction between alpha-keto acids and internal alkynes using Rhodamine 6G as photocatalyst. Various kinds of substrates are suitable for this methodology, affording the corresponding indenones in a greener and efficient manner. An efficient photocatalysis has been developed for the synthesis of indanone using low-energy green light as input energy. This methodology provides a greener avenue to construct indanone through a metal-free photocatalytic radical annulation reaction between alpha-keto acid and internal alkyne. image
引用
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页数:5
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