L
Liu-Zhu Gong
Researcher at University of Science and Technology of China
Publications - 106
Citations - 4029
Liu-Zhu Gong is an academic researcher from University of Science and Technology of China. The author has contributed to research in topics: Enantioselective synthesis & Catalysis. The author has an hindex of 30, co-authored 103 publications receiving 3174 citations. Previous affiliations of Liu-Zhu Gong include Center for Excellence in Education & Chinese Academy of Sciences.
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Catalytic Generation of C1 Ammonium Enolates from Halides and CO for Asymmetric Cascade Reactions
TL;DR: A general strategy for the design of asymmetric cascade reactions using readily available halides and carbon monoxide (CO) as substrates is developed and asymmetric formal [1+1+4] and [1-1+2] reactions are established to afford chiral dihydropyridones and β-lactams with high yields and high enantio- and diastereoselectivities.
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Enantioselective Synthesis of 5-Alkylated Thiazolidinones via Palladium-Catalyzed Asymmetric Allylic C-H Alkylations of 1,4-Pentadienes with 5 H-Thiazol-4-ones.
TL;DR: A palladium-catalyzed, enantioselective allylic C-H alkylation of 1,4-pentadienes with 5 H-thiazol-4-ones has been developed and led to linear and branched allylation products, respectively.
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Recent Progress in Asymmetric Relay Catalysis of Metal Complex with Chiral Phosphoric Acid
TL;DR: This chapter will mainly highlight progress from 2014 to mid-2019 in asymmetric relay catalysis of metal complex with chiral phosphoric acid, which has grown rapidly since 2008.
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Monodentate Phosphorus Ligand-Enabled General Palladium-Catalyzed Allylic C-H Alkylation of Terminal Alkenes.
TL;DR: Mechanistic studies suggest that a ternary Pd(0) complex, coordinated with a monodentate phosphorus ligand, benzoquinone, and alkene, is most likely to be an active species.
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Asymmetric α-Allylation of Aldehydes with Alkynes by Integrating Chiral Hydridopalladium and Enamine Catalysis
TL;DR: A palladium-catalyzed asymmetric α-allylation of aldehydes with alkynes has been established by integrating the catalysis of enamine and chiral hydridopalladium complex that is reversibly formed from the oxidative addition of Pd(0) to chiral phosphoric acid.