Cu(ii)-Mediated aerobic oxidative synthesis of sulfonated chromeno[4,3-c]pyrazol-4(2H)-ones

被引:6
作者
Zhou, Quan [1 ,2 ]
Yu, Hai-Yan [1 ,2 ]
Zhou, Yaqing [3 ]
Wei, Jing-Ru [1 ,2 ]
Wang, Lei [1 ,2 ,4 ]
机构
[1] Taizhou Univ, Adv Res Inst, Taizhou 318000, Zhejiang, Peoples R China
[2] Taizhou Univ, Dept Chem, Taizhou 318000, Zhejiang, Peoples R China
[3] Taizhou Jiaxin Metering & Testing Co Ltd, Dept Chem, Taizhou 317000, Zhejiang, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
SELECTIVE INHIBITORS; DERIVATIVES; CYCLIZATION; DISCOVERY; COUMARIN; CARBONYL; LIGANDS; POTENT;
D O I
10.1039/d2ob00639a
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Herein, starting with propiolates and sulfonyl hydrazides, we developed a concise and facile synthesis of 2-sulfonylated chromeno [4,3-c]pyrazol-4(2H)-ones or 2,5-dihydro-4H-pyrazolo[4,3-c]quinolin-4-ones via Cu(ii)-promoted oxidative cascade C-C/C-N bond formation. This protocol has the advantages of atom economy and good functional group tolerance. The primary mechanism studies indicate that the reaction involves a free-radical process as well as terminal alkyne C-H activation.
引用
收藏
页码:5575 / 5581
页数:7
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