Z
Zhengkun Yu
Researcher at Chinese Academy of Sciences
Publications - 236
Citations - 7372
Zhengkun Yu is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Catalysis & Ketene. The author has an hindex of 45, co-authored 236 publications receiving 6356 citations. Previous affiliations of Zhengkun Yu include Iowa State University & Dalian Institute of Chemical Physics.
Papers
More filters
Journal ArticleDOI
Multiple reactivities of dithranol towards 1-alkynyl Fischer carbene complexes (CO) 5 M@C(OEt)C"CPh (M = Cr, W) - Efficient chemical synthesis of aromatic polyketides
Ning Luo,Zhengkun Yu,Zhengkun Yu +2 more
TL;DR: In this paper, the reaction of anti-psoriasis drug dithranol with 1-alkynyl Fischer carbene complexes (CO)5M C(OEt)C CPh (M = Cr, W) was investigated under controlled conditions.
Journal ArticleDOI
Copper(II)-Mediated Dehydrogenative Cross-Coupling of Heteroarenes.
TL;DR: In this paper, an efficient and environmentally friendly method to prepare various unsymmetrical biheteroarenes is proposed, which provides an efficient method to deal with the problem of energy consumption.
Journal ArticleDOI
Visible-Light-Driven, Palladium-Catalyzed Heck Reaction of Internal Vinyl Bromides with Styrenes.
Yunlong Li,Haibo Liu,Zilong Huang,Zilong Huang,Yuan He,Yuan He,Bao-Hua Xu,Hongmei Wang,Zhengkun Yu,Zhengkun Yu +9 more
TL;DR: In this article, a Heck reaction of S,S-functionalized internal vinyl bromides with styrenes under mild conditions was used to obtain functionalized 1,3-dienes.
Journal ArticleDOI
Brønsted Acid-Catalyzed Phenylselenenylation of Internal Olefins
TL;DR: In this article, the authors used N-phenylselenophthalimide (N-PSP) as the reagent for the phenylseleno reagent, and the resultant selenated ketene dithioacetals reacted with styrene in the presence of the same acid to undergo PhSe group transfer, regioselectively affording Markovnikov type PhSe-alkylated olefins.
Journal ArticleDOI
Copper(II)-Mediated Intramolecular Cyclopropanation of Ketene N,X-Acetals (X = S, O, N) under Mild Conditions.
TL;DR: CuBr2-mediated intramolecular oxidative cyclopropanation of α-oxo ketene N,S-acetals was efficiently achieved to afford 2-thioalkyl-3-azabicyclo-[3.1.0]hexenes under mild conditions.