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Xin Cui

Researcher at Chinese Academy of Sciences

Publications -  181
Citations -  5938

Xin Cui is an academic researcher from Chinese Academy of Sciences. The author has contributed to research in topics: Catalysis & Enantioselective synthesis. The author has an hindex of 40, co-authored 161 publications receiving 5110 citations. Previous affiliations of Xin Cui include Tsinghua University & University of Science and Technology of China.

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Novel Small Organic Molecules for a Highly Enantioselective Direct Aldol Reaction

TL;DR: A theoretical study of transition structures demonstrates the important role of the terminal hydroxyl group in the catalyst in the stereodiscrimination and suggests a new strategy in the design of new organic catalysts for direct asymmetric aldol reactions and related transformations because plentiful chiral resources containing multi-hydrogen bond donors, for example, peptides, might be adopted in the designs.
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Enantioselective direct aldol reactions catalyzed by L-prolinamide derivatives.

TL;DR: A new strategy in the design of new organic catalysts for direct asymmetric aldol reactions and related transformations is suggested as the calculations reveal that the amide N-H and the terminal hydroxyl groups form hydrogen bonds with the benzaldehyde substrate that cause high enantioselectivity.
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Copper-catalyzed synthesis of aryl azides and 1 -aryl -1,2,3 -triazoles from boronic acids

TL;DR: A new one-pot procedure was developed to synthesize 1-aryl- and 1-vinyl-1,2,3-triazoles directly from boronic acids and alkynes, which avoided the need to isolate unstable azide intermediates.
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Formation of silver nanowires by a novel solid-liquid phase arc discharge method

TL;DR: In this article, a novel technique for fabrication of silver nanowires was successfully developed via a so-called solid−liquid phase arc discharge method (SLPAD), which was found that the aging time following the SLPAD method has a significant effect on the formation and growth of silver nano-wires.
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Asymmetric Transfer Hydrogenation of Prochiral Ketones in Aqueous Media with New Water-Soluble Chiral Vicinal Diamine as Ligand

TL;DR: An easily accessible water-soluble chiral o-sulfonated 1,2-diphenylethlenediamine 2 and its mono-N-tosylated derivative 3 were synthesized for the first time.