His scientific interests lie mostly in Organic chemistry, Enantioselective synthesis, Catalysis, Organocatalysis and Stereochemistry. His Enantioselective synthesis research includes elements of Thiourea, Bifunctional, Stereoisomerism, Michael reaction and Polymer supported. His Thiourea research is multidisciplinary, relying on both Tertiary amine and Medicinal chemistry.
The various areas that Rui Wang examines in his Michael reaction study include Phosphonate, Zinc and Reaction conditions. His research integrates issues of Combinatorial chemistry and Ligand in his study of Catalysis. His biological study spans a wide range of topics, including Antimicrobial, Stereocenter and Cytotoxicity.
His primary areas of study are Catalysis, Enantioselective synthesis, Organic chemistry, Organocatalysis and Combinatorial chemistry. Rui Wang interconnects Thiourea, Amino acid, Yield, Medicinal chemistry and Ligand in the investigation of issues within Catalysis. His Thiourea study combines topics from a wide range of disciplines, such as Tertiary amine and Cinchona.
His Enantioselective synthesis research incorporates elements of Bifunctional, Addition reaction, Stereochemistry and Michael reaction. His Organocatalysis research is multidisciplinary, incorporating elements of Cascade reaction, Oxindole and Primary. As part of the same scientific family, Rui Wang usually focuses on Combinatorial chemistry, concentrating on Magnesium and intersecting with Intermolecular force.
Catalysis, Enantioselective synthesis, Combinatorial chemistry, Organic chemistry and Medicinal chemistry are his primary areas of study. His Catalysis study integrates concerns from other disciplines, such as Ligand and Magnesium. He does research in Enantioselective synthesis, focusing on Organocatalysis specifically.
His Organocatalysis research is multidisciplinary, incorporating perspectives in Yield and Oxindole. His work deals with themes such as Chiral ligand, Aryl and Transition metal, which intersect with Combinatorial chemistry. His Medicinal chemistry research incorporates themes from Intramolecular force, Alkene, Michael reaction and Addition reaction.
Rui Wang focuses on Enantioselective synthesis, Organic chemistry, Catalysis, Stereochemistry and Combinatorial chemistry. His studies in Enantioselective synthesis integrate themes in fields like Bifunctional, Imine, Rhodium, Ring and Oxindole. His research links Oxidative phosphorylation with Organic chemistry.
Rui Wang works in the field of Catalysis, namely Organocatalysis. His Stereochemistry research integrates issues from Stereocenter, Ketene, Phosphonic acid derivatives, Molecule and Phosphorylation. His Combinatorial chemistry research focuses on Chiral ligand and how it relates to In situ and Amino acid.
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Recent Advances in Asymmetric Organocatalytic Construction of 3,3′‐Spirocyclic Oxindoles
Liang Hong;Rui Wang;Rui Wang.
Advanced Synthesis & Catalysis (2013)
Enantioselective Michael/cyclization reaction sequence: scaffold-inspired synthesis of spirooxindoles with multiple stereocenters.
Yiming Cao;Xianxing Jiang;Luping Liu;Fangfang Shen.
Angewandte Chemie (2011)
Recent developments in metal catalyzed asymmetric addition of phosphorus nucleophiles
Depeng Zhao;Rui Wang.
Chemical Society Reviews (2012)
Montmorillonite K-10: An efficient and reusable catalyst for the synthesis of quinoxaline derivatives in water
Tai-kun Huang;Rui Wang;Lin Shi;Xiao-xia Lu.
Catalysis Communications (2008)
An organocatalytic cascade strategy for the enantioselective construction of spirocyclopentane bioxindoles containing three contiguous stereocenters and two spiro quaternary centers.
Wangsheng Sun;Gongming Zhu;Chongyang Wu;Liang Hong.
Chemistry: A European Journal (2012)
Catalytic Asymmetric Michael Addition/Cyclization of Isothiocyanato Oxindoles: Highly Efficient and Versatile Approach for the Synthesis of 3,2′‐Pyrrolidinyl Mono‐ and Bi‐spirooxindole Frameworks
Yi-Ming Cao;Fang-Fang Shen;Fu-Ting Zhang;Rui Wang;Rui Wang.
Chemistry: A European Journal (2013)
Antitumor effects, cell selectivity and structure–activity relationship of a novel antimicrobial peptide polybia-MPI
Kai-rong Wang;Bang-zhi Zhang;Bang-zhi Zhang;Wei Zhang;Jie-xi Yan.
Highly Enantioselective Synthesis of γ-Nitro Heteroaromatic Ketones in a Doubly Stereocontrolled Manner Catalyzed by Bifunctional Thiourea Catalysts Based on Dehydroabietic Amine: A Doubly Stereocontrolled Approach to Pyrrolidine Carboxylic Acids
Xianxing Jiang;Yifu Zhang;Albert S. C. Chan;Rui Wang.
Organic Letters (2009)
The highly enantioselective addition of indoles and pyrroles to isatins-derived N-Boc ketimines catalyzed by chiral phosphoric acids.
Jingchao Feng;Wenjin Yan;Dong Wang;Peng Li.
Chemical Communications (2012)
NbCl5-catalyzed one-pot mannich-type reaction : three component synthesis of β-amino carbonyl compounds
Rui Wang;Bo-gang Li;Tai-kun Huang;Lin Shi.
Tetrahedron Letters (2007)
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