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Shu-Jiang Tu
Researcher at Jiangsu Normal University
Publications - 604
Citations - 10937
Shu-Jiang Tu is an academic researcher from Jiangsu Normal University. The author has contributed to research in topics: Catalysis & Ring (chemistry). The author has an hindex of 51, co-authored 593 publications receiving 9428 citations. Previous affiliations of Shu-Jiang Tu include Texas Tech University.
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Journal ArticleDOI
Multicomponent Reactions for the Synthesis of Heterocycles
TL;DR: Recent advances on multicomponent domino reactions for the construction of five-, six-, and seven-membered heterocyclic skeletons and their multicyclic derivatives are covered.
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Catalytic Dual 1,1-H-Abstraction/Insertion for Domino Spirocyclizations
Jiang-Kai Qiu,Jiang-Kai Qiu,Bo Jiang,Yi-Long Zhu,Yi-Long Zhu,Wen-Juan Hao,De-Cai Wang,Jun Sun,Jun Sun,Ping Wei,Shu-Jiang Tu,Guigen Li +11 more
TL;DR: A catalytic domino spirocyclization of 1,7-enynes with simple cycloalkanes and cyclo-1,3-dicarbonyls has been established via multiple C-C bond formations from alkynyl/alkenyl functions and dual α,α-C(sp(3))-H abstraction/insertion.
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Merging [2+2] Cycloaddition with Radical 1,4-Addition: Metal-Free Access to Functionalized Cyclobuta[a]naphthalen-4-ols.
Feng Liu,Jia-Yin Wang,Peng Zhou,Guigen Li,Guigen Li,Wen-Juan Hao,Shu-Jiang Tu,Bo Jiang,Bo Jiang +8 more
TL;DR: A metal-free cycloaddition and 1,4-addition sequence induced by S-centered radicals has been achieved by treating benzene-linked allene-ynes with aryldiazonium tetrafluoroborates and DABCO-bis(sulfur dioxide) in a one-pot procedure, providing a greener and more practical access to functionalized cyclobuta[a]naphthalen-4-ols with valuable applications.
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Diastereo- and Enantioselective Construction of 3,3'-Pyrrolidinyldispirooxindole Framework via Catalytic Asymmetric 1,3-Dipolar Cycloadditions.
TL;DR: The first catalytic enantioselective construction of a 3,3'-pyrrolidinyldispirooxindole scaffold has been established via organocatalytic asymmetric 1,3-dipolar cycloadditions of isatin-derived azomethine ylides with methyleneindolinones.
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Recent advances in radical transformations of internal alkynes
TL;DR: This review highlights the recent progress in this rapidly growing area by presenting a series of catalytic oxidative reactions, mechanisms and applications which have appeared in the most recent literature.