His scientific interests lie mostly in Enantioselective synthesis, Organic chemistry, Catalysis, Stereocenter and Organocatalysis. His Enantioselective synthesis study combines topics from a wide range of disciplines, such as Bifunctional, Phosphoric acid, Michael reaction, Oxindole and Stereochemistry. In his research, Tertiary amine is intimately related to Thiourea, which falls under the overarching field of Bifunctional.
Wei-Cheng Yuan frequently studies issues relating to Amine gas treating and Catalysis. Within one scientific family, he focuses on topics pertaining to Yield under Stereocenter, and may sometimes address concerns connected to Vicinal and Cycloaddition. His Organocatalysis research is multidisciplinary, incorporating perspectives in Lewis acids and bases and Hydrosilylation.
His primary areas of investigation include Catalysis, Organic chemistry, Enantioselective synthesis, Combinatorial chemistry and Organocatalysis. His work in Catalysis addresses subjects such as Medicinal chemistry, which are connected to disciplines such as Domino. His Enantioselective synthesis research includes themes of Bifunctional, Stereochemistry and Michael reaction.
Wei-Cheng Yuan combines subjects such as Tertiary amine, Nitro and Amine gas treating with his study of Bifunctional. His Combinatorial chemistry research integrates issues from Substituent and Cascade reaction. His work in Stereocenter tackles topics such as Cycloaddition which are related to areas like Isoxazole.
Wei-Cheng Yuan spends much of his time researching Catalysis, Organic chemistry, Enantioselective synthesis, Combinatorial chemistry and Cycloaddition. Wei-Cheng Yuan is interested in Bifunctional, which is a branch of Catalysis. He studies Enantioselective synthesis, focusing on Stereocenter in particular.
Wei-Cheng Yuan has included themes like Aromatization, Annulation, Michael reaction, Derivative and Substituent in his Combinatorial chemistry study. His work carried out in the field of Cycloaddition brings together such families of science as Oxazoline, Isoxazole, Oxindole and Stereoselectivity. Wei-Cheng Yuan has researched Oxindole in several fields, including Aldol reaction, Molecule and Stereochemistry.
Wei-Cheng Yuan mainly investigates Catalysis, Cycloaddition, Enantioselective synthesis, Organic chemistry and Stereocenter. The concepts of his Catalysis study are interwoven with issues in Yield, Thiourea and Trifluoromethyl. The study incorporates disciplines such as Annulation, Oxindole, Sulfur and Medicinal chemistry in addition to Cycloaddition.
His Enantioselective synthesis research incorporates themes from Bifunctional, Zinc, Combinatorial chemistry and Mannich reaction. Indoline and Nucleophilic substitution are among the areas of Organic chemistry where the researcher is concentrating his efforts. His Stereocenter research is multidisciplinary, relying on both Oxazoline and Stereoselectivity.
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Highly Enantioselective Construction of Spiro[4H-pyran-3,3′-oxindoles] Through a Domino Knoevenagel/Michael/Cyclization Sequence Catalyzed by Cupreine
Wen-Bing Chen;Zhi-Jun Wu;Qing-Lan Pei;Lin-Feng Cun.
Organic Letters (2010)
Organocatalytic Direct Asymmetric Aldol Reactions of 3-Isothiocyanato Oxindoles to Ketones: Stereocontrolled Synthesis of Spirooxindoles Bearing Highly Congested Contiguous Tetrasubstituted Stereocenters
Wen-Bing Chen;Zhi-Jun Wu;Jing Hu;Lin-Feng Cun.
Organic Letters (2011)
Highly efficient and stereocontrolled construction of 3,3'-pyrrolidonyl spirooxindoles via organocatalytic domino Michael/cyclization reaction.
Xiong-Li Liu;Wen-Yong Han;Xiao-Mei Zhang;Wei-Cheng Yuan.
Organic Letters (2013)
Highly diastereo- and enantioselective Michael additions of 3-substituted oxindoles to maleimides catalyzed by chiral bifunctional thiourea-tertiary amine.
Yu-Hua Liao;Xiong-Li Liu;Zhi-Jun Wu;Lin-Feng Cun.
Organic Letters (2010)
Organocatalytic Asymmetric Michael Addition of Pyrazolin-5-ones to Nitroolefins with Bifunctional Thiourea: Stereocontrolled Construction of Contiguous Quaternary and Tertiary Stereocenters
Yu-Hua Liao;Wen-Bing Chen;Zhi-Jun Wu;Xi-Lin Du.
Advanced Synthesis & Catalysis (2010)
FeCl3-catalyzed stereoselective construction of spirooxindole tetrahydroquinolines via tandem 1,5-hydride transfer/ring closure.
Yan-Yan Han;Wen-Yong Han;Xue Hou;Xiao-Mei Zhang.
Organic Letters (2012)
Asymmetric Michael/cyclization cascade reaction of 3-isothiocyanato oxindoles and 3-nitroindoles with amino-thiocarbamate catalysts: enantioselective synthesis of polycyclic spirooxindoles.
Jian-Qiang Zhao;Ming-Qiang Zhou;Zhi-Jun Wu;Zhen-Hua Wang.
Organic Letters (2015)
Highly Enantioselective [3+2] Coupling of Indoles with Quinone Monoimines Promoted by a Chiral Phosphoric Acid
Lihua Liao;Chang Shu;Minmin Zhang;Yijun Liao.
Angewandte Chemie (2014)
3‐Isothiocyanato Oxindoles Serving as Powerful and Versatile Precursors to Structurally Diverse Dispirocyclic Thiopyrrolidineoxindoles through a Cascade Michael/Cyclization Process with Amino‐Thiocarbamate Catalysts
Wen-Yong Han;Shi-Wu Li;Zhi-Jun Wu;Xiao-Mei Zhang.
Chemistry: A European Journal (2013)
Organocatalytic enantioselective hydroxymethylation of oxindoles with paraformaldehyde as C1 unit.
Xiong-Li Liu;Yu-Hua Liao;Zhi-Jun Wu;Lin-Feng Cun.
Journal of Organic Chemistry (2010)
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