K
Kezuan Deng
Researcher at East China University of Science and Technology
Publications - 7
Citations - 61
Kezuan Deng is an academic researcher from East China University of Science and Technology. The author has contributed to research in topics: Catalysis & Oxime. The author has an hindex of 3, co-authored 7 publications receiving 27 citations.
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Journal ArticleDOI
Tandem C-C/C-N Formation via Palladium-Catalyzed C-H Activation/Styrenation and Sequential Annulation of O-Methylketoxime with Styrenes.
TL;DR: A novel route for tandem C-C/C-N formation via palladium-catalyzed C-H activation/styrenation and annulation of O-methylketoxime with styrenes to synthesize benzothienopyridine and benzofuropyridines has been developed.
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C-H Borylation of Diphenylamines through Adamantane-1-carbonyl Auxiliary by BBr3.
TL;DR: A method for ortho-C-H borylation of diphenylamines using BBr3 as the boron source has been reported and the noncatalytic adamantane-1-carbonyl directed reaction exhibited site exclusivity and good functional group tolerance.
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Ruthenium(II)-Catalyzed α-Fluoroalkenylation of Oxime Ethers with gem-Difluorostyrenes via C-H Activation and C-F Cleavage.
Li-Li Zhang,Kezuan Deng,Gaorong Wu,Jinyue Yang,Shi-Biao Tang,Xiao-Pan Fu,Chengcai Xia,Ya-Fei Ji +7 more
TL;DR: A novel route for Ruthenium(II)-catalyzed α-fluoroalkenylation of oxime ethers with gem-difluorostyrenes via C-H activation and C-F cleavage has been firstly developed.
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Rhodium(III)-catalyzed C4-amidation of indole-oximes with dioxazolones via C-H activation.
Shi-Biao Tang,Xiao-Pan Fu,Gaorong Wu,Li-Li Zhang,Kezuan Deng,Jinyue Yang,Chengcai Xia,Ya-Fei Ji +7 more
TL;DR: A novel method for the Rh(iii)-catalyzed oxime-directed C-H amidation of indoles with dioxazolones has been developed and may serve as a significant tool to construct structurally diverse indole derivatives for the screening of potential pharmaceuticals in the future.
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2-Amino-5,6-difluorophenyl-1H-pyrazole-Directed PdII Catalysis: Arylation of Unactivated β-C(sp3)-H Bonds.
TL;DR: Palladium-catalyzed arylation of unactivated β-C(sp3)-H bonds in carboxylic acid derivatives with aryl iodides is described for the first time using 2-amino-5,6-difluorophenyl-1H-pyrazole as an efficient and readily removable directing group.