financial support from the National Natural Science Foundation of China(Nos.22261013 and 22001049);Guangxi Natural Science Foundation(No.2020GXNSFBA297003);Magneto-Chemical Functional Materials(No.EMFM20221102)。
Rhodium-catalyzed C4aryl-H activation and ring-retentive annulation of 2H-imidazoles with internal alkynes to build imidazo[5,1-a]isoquinolinium salts with high yields and broad scope has been disclosed.These novel sa...
Project supported by the Scientific Research Foundation of Hunan Provincial Education Department(No.23B0650);the Natural Science Foundation of Hunan Province(No.2022JJ30418);the Key Scientific Research Foundation of Hunan University of Arts and Science(No.22ZD04);the Innovation and Entrepreneurship Training Program for College Students of Hunan University of Arts and Science(No.XDC202318)。
An efficient visible-light-induced radical cascade azidation/cyclization of 2-aryl indoles with trimethylsilyl azide(TMSN3)has been developed using organic dye Rose Bengal as the photocatalyst.This method did not requ...
the Tianshan Talents Program for Leading Talents in Science and Technology Innovation(No.2022TSYCLJ0016);the National Natural Science Foundation of China(Nos.21961037 and 22201241);the Program for Tianshan Innovative Research Team of Xinjiang Uygur Autonomous Region(No.2021D14011);the Graduate Innovation Project of Xinjiang Uygur Autonomous Region(No.XJ2021G036);the Key Program of Natural Science Foundation of Xinjiang Uygur Autonomous Region(No.2022D01D06);the Natural Science Foundation of Xinjiang Uygur Autonomous Region(Nos.2021D01E10 and 2022E01042).
Photocatalytic and photoinduced silyl radicals cascade cyclization procedures for the green and simple preparation of fused tetracyclic skeleton silylated indolo[2,1-a]isoquinoline-6(5H)-ones from 2-aryl-N-acryloyl in...
We thank the National Key R&D Program of China(2021YFA1500100);National Natural Science Foundation of China(21821002,92256302,22071260);Science and Technology Commission of Shanghai Municipality(21520780100)for generous financial support.S.-L.Y.thanks the supports from the New Cornerstone ScienceFoundation.
Rhodium(III)-catalyzed enantioselective C-H indolylization of isoquinolines was developed.The C-H coupling reactions between 1-aryl isoquinoline derivatives and 3-indolylphenyliodonium salts proceeded smoothly in the ...
the financial supports from the Joint Funds of the Zhejiang Provincial Natural Science Foundation of China(No.LTY21B020001);the Fundamental Research Funds of Zhejiang Sci-Tech University(No.2021Q052)。
A novel palladium-catalyzed carbonylative cyclization of alkene-tethered indoles with phenols or arylboronic acids is described,which provides a facile approach to access indolo[2,1-a]isoquinoline scaffolds.This metho...
Foundation of the National Natural Science Foundation of China(No.22101212);“Climbing Program”(No.pdjh2021a0505)Special Funds;Science Foundation for Young Teachers of Wuyi University(No.2019td06);Guangdong Basic and Applied Basic Research Foundation(Nos.2019A1515110866,2019A1515110522);College Students Innovation and Entrepreneurship Training Program of Wuyi University(Nos.202111349020,202111349308S)for financial support。
In this study,a method was developed to form C(sp^(3))-C(sp^(2))bonds via copper catalyst-promoted cross coupling of 2-methylquinoline and in-situ-activated 3-haloisoquinoline under mild conditions.The multi-component...
financially supported by the National Natural Science Foundation of China(21701122 and 21871206)。
The rational design and synthesis of hierarchically hollow nanostructures with controlled spatial architecture and composition are significant in electrocatalysis owing to their abundant active sites and the expedited...
Istituto Italiano di Tecnologia and the University of Genova are gratefully acknowledged for financial support;the COST Action CA 15107“Multi-Functional Nano-Carbon Composite Materials Network(MultiComp)”。
The search for new fluorescent molecules for possible applications as functional p-electron systems and their conjugation with different nanomaterials is nowadays of paramount importance to broaden the availability of...
The generous financial support from the National Natural Science Foundation of China (Nos. 21372070 and 21471052) and the Hunan Provincial Education Department Scientific Research Fund (No. 14k035) are gratefully acknowledged.
An operationally simple approach for the tandem synthesis of isoquinolines by the reaction of o-alkynylalde- hydes with ammonium bicarbonate via Ag-catalyzed 6-endo-dig ring closure is described. The reaction conditio...
supported by the Dalian Institute of Chemical Physics,Chinese Academy of Sciences;the National Natural Science Foundation of China (21272231)~~
A redox‐neutral avenue to access isoquinolines has been realized by a Co(III)‐catalyzed C–H activa‐tion process. Starting from readily available N‐sulfinyl imine substrates and alkynes, the reaction occurred vi...