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Liu-Zhu Gong

Researcher at University of Science and Technology of China

Publications -  61
Citations -  3508

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 29, co-authored 61 publications receiving 3340 citations. Previous affiliations of Liu-Zhu Gong include Chinese Academy of Sciences & Nankai University.

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Highly Diastereo- and Enantioselective Direct Aldol Reactions of Cycloketones with Aldehydes Catalyzed by a trans-4-tert-Butyldimethylsiloxy-L-proline Amide.

TL;DR: In this article, an organocatalyst derived from trans-4-hydroxy- l -proline and (1S,2S)-1,2-diphenyl-2-aminoethanol catalyzes the direct aldol reactions of cycloketones with a wide scope of aldehydes in high yields and with excellent diastereoselectivities of up to >99:1 and enanti-lectivities up to 99% ee.
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Palladium‐Catalyzed Allylic Alkylation of tert‐Butyl(diphenylmethylene)‐glycinate with Simple Allyl Esters under Chiral Phase Transfer Conditions.

TL;DR: The first example of palladium-catalyzed allylic alkylation of an imino ester with simple allyl esters in the presence of a chiral quaternary ammonium salt is reported in this paper.
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Organo-Catalyzed Highly Diastereo- and Enantio-Selective Direct Aldol Reactions in Water.

TL;DR: In this paper, the asymmetric direct aldol reactions of a wide scope of aromatic aldehydes, with unmodified ketones in the presence of 1 ǫ% of organocatalyst prepared from (2 R, 3 R )-diethyl 2-amino-3-hydroxysuccinate and trans -4-hydroxy- l -proline, were performed in water.
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The First Use of Chiral Oxazoline Ligands in the Highly Enantioselective Diethylzinc Addition to Diphenylphosphinoyl Imines.

TL;DR: A series of chiral oxazolines, which had been conveniently prepared from commercially available (1S,2S)-2-amino-1-phenylpropane-1,3-diol, was applied in the diethylzinc addition to diphenylphosphinoyl imines to give high yields of 68-84% and excellent e.g. values of 90-93% as mentioned in this paper.
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Asymmetric Direct Aldol Reaction Catalyzed by an L-Prolinamide Derivative: Considerable Improvement of the Catalytic Efficiency in the Ionic Liquid.

TL;DR: In this article, the asymmetric direct aldol reactions of a wide scope of aldehydes with unmodified ketones in the presence of 20 mol% increase in the number of modifications was performed in ionic liquids.