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Xin-Yuan Liu
Researcher at Southern University of Science and Technology
Publications - 179
Citations - 7055
Xin-Yuan Liu is an academic researcher from Southern University of Science and Technology. The author has contributed to research in topics: Catalysis & Enantioselective synthesis. The author has an hindex of 47, co-authored 153 publications receiving 5288 citations. Previous affiliations of Xin-Yuan Liu include Zhejiang University & South University of Science and Technology of China.
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Recent advances in copper-catalysed radical-involved asymmetric 1,2-difunctionalization of alkenes
TL;DR: This tutorial review highlights the recent progress in copper-catalysed radical-involved asymmetric 1,2-difunctionalization of alkenes and the mechanistic scenarios governing the stereocontrol, with an emphasis on utilization of chiral ligands.
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Phosphine gold(I)-catalyzed hydroamination of alkenes under thermal and microwave-assisted conditions.
TL;DR: This is the first example of the use of microwave radiation as a heat source for gold(I)-catalyzed organic reactions, catalyzed isomerization of terminal alkenes and hydroamination of unactivatedAlkenes under thermal and microwave-assisted conditions.
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Atroposelective Synthesis of Axially Chiral Biaryldiols via Organocatalytic Arylation of 2-Naphthols.
TL;DR: The first phosphoric acid-catalyzed asymmetric direct arylative reactions of 2-naphthols with quinone derivatives have been developed, providing efficient access to a class of axially chiral biaryldiols in good yields with excellent enantioselectivities under mild reaction conditions.
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A Dual-Catalytic Strategy To Direct Asymmetric Radical Aminotrifluoromethylation of Alkenes
TL;DR: A novel asymmetric radical aminotrifluoromethylation of alkenes has been developed for the first time, providing straightforward access to densely functionalized CF3-containing azaheterocycles bearing an α-tertiary stereocenter with excellent enantioselectivity.
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Synthesis of Substituted 1,2-Dihydroquinolines and Quinolines from Aromatic Amines and Alkynes by Gold(I)-Catalyzed Tandem Hydroamination−Hydroarylation under Microwave-Assisted Conditions
TL;DR: A method to efficiently prepare substituted 1,2-dihydroquinolines and quinolines by Au(I)-catalyzed tandem hydroamination-hydroarylation under microwave irradiation was developed and has a broad substrate scope.