详细信息
Graphitic Carbon Nitride Polymer as a Recyclable Photoredox Catalyst for Decarboxylative Alkynylation of Carboxylic Acids ( SCI-EXPANDED收录)
文献类型:期刊文献
英文题名:Graphitic Carbon Nitride Polymer as a Recyclable Photoredox Catalyst for Decarboxylative Alkynylation of Carboxylic Acids
作者:Guo, Jiaqi[1,2];Wang, Yating[3];Li, Yuhang[3];Lu, Kailin[1,2];Liu, Shihui[1,2];Wang, Wei[1,2,4,5];Zhang, Yongqiang[1,2]
机构:[1]East China Univ Sci & Technol, State Key Lab Bioreactor Engn, Shanghai Key Lab New Drug Design, Shanghai 200237, Peoples R China;[2]East China Univ Sci & Technol, Sch Pharm, Shanghai 200237, Peoples R China;[3]East China Univ Sci & Technol, Sch Mat Sci & Engn, Shanghai Engn Res Ctr Hierarch Nanomat, Key Lab Ultrafine Mat,Minist Educ, Shanghai 200237, Peoples R China;[4]Univ Arizona, Dept Pharmacol & Toxicol, Tucson, AZ 85721 USA;[5]Univ Arizona, Inst BIO5, Tucson, AZ 85721 USA
年份:2020
卷号:362
期号:18
起止页码:3898
外文期刊名:ADVANCED SYNTHESIS & CATALYSIS
收录:;WOS:【SCI-EXPANDED(收录号:WOS:000555570600001),CCR-EXPANDED(收录号:WOS:000555570600001)】;
基金:Financial support from the program of the National Natural Science Foundation of China (21871086, Y.-Q. Z.; 21738002, W. W.) is gratefully acknowledged.
语种:英文
外文关键词:graphitic carbon nitride; heterogeneous photoredox catalysis; decarboxylative alkynylation; sustainable synthesis
摘要:Visible-light-induced heterogeneous photocatalysis for decarboxylative alkynylation has been performed. The using of cheap, metal-free and recyclable graphitic carbon nitride (g-C3N4) as the photoredox catalyst in the process enables the facile transformation of a variety of carboxylic acids into structurally diverse alkyne-containing molecular architectures under mild and environmentally-benign conditions. Notably, the heterogeneous nature of the reaction system allows for the recovery and reuse of the catalyst in multiple runs without loss of reactivity. The photocatalytic reactions could also be performed in a continuous flow fashion and scaled up to gram-scale. Furthermore, the preparative power of this strategy is further highlighted by its application in the 1, 2-amido alkynylation of unactivated alkenes.
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