His scientific interests lie mostly in Catalysis, Organic chemistry, Enantioselective synthesis, Combinatorial chemistry and Allylic rearrangement. His Catalysis study incorporates themes from Intramolecular force and Ligand. The study incorporates disciplines such as Indole test, Medicinal chemistry, Michael reaction and Stereoisomerism in addition to Enantioselective synthesis.
His Combinatorial chemistry study combines topics in areas such as Yield, Rhodium, Aryl and Oxidative coupling of methane. His studies in Allylic rearrangement integrate themes in fields like Total synthesis, Nucleophile and Substitution reaction. Shu-Li You combines subjects such as Amination and Stereochemistry with his study of Tsuji–Trost reaction.
His primary areas of study are Catalysis, Enantioselective synthesis, Organic chemistry, Combinatorial chemistry and Allylic rearrangement. His biological study spans a wide range of topics, including Indole test, Intramolecular force and Medicinal chemistry. His Enantioselective synthesis study integrates concerns from other disciplines, such as Ligand and Stereochemistry.
His Organic chemistry study focuses mostly on Friedel–Crafts reaction, Phosphoric acid, Yield, Alkylation and Reaction conditions. Shu-Li You has researched Combinatorial chemistry in several fields, including Copper and Indoline. Shu-Li You has included themes like Amination, Regioselectivity, Substitution reaction, Intermolecular force and Nucleophile in his Allylic rearrangement study.
Catalysis, Enantioselective synthesis, Combinatorial chemistry, Medicinal chemistry and Indole test are his primary areas of study. His Catalysis research incorporates themes from Aryl, Intramolecular force and Intermolecular force. His Enantioselective synthesis research incorporates elements of Rhodium, Nucleophile and Copper.
His studies deal with areas such as Ligand, Molecule, Optically active, Organic synthesis and Indoline as well as Combinatorial chemistry. His research integrates issues of Yield, Alkylation, β naphthol and Tsuji–Trost reaction in his study of Medicinal chemistry. His Allylic rearrangement research entails a greater understanding of Organic chemistry.
Shu-Li You spends much of his time researching Catalysis, Combinatorial chemistry, Enantioselective synthesis, Indole test and Medicinal chemistry. The Catalysis study combines topics in areas such as Photochemistry and Aryl. His specific area of interest is Enantioselective synthesis, where Shu-Li You studies Organocatalysis.
Shu-Li You interconnects Chemical physics, Total synthesis, Intramolecular force and Stereocenter in the investigation of issues within Indole test. His work in the fields of Medicinal chemistry, such as Isoquinoline, intersects with other areas such as Surface modification. His Electrophile study improves the overall literature in Organic chemistry.
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Catalytic Asymmetric Dearomatization Reactions
Chun-Xiang Zhuo;Wei Zhang;Shu-Li You.
Angewandte Chemie (2012)
Chiral Bronsted acid catalyzed Friedel-Crafts alkylation reactions
Shu-Li You;Quan Cai;Mi Zeng.
Chemical Society Reviews (2009)
Asymmetric Catalysis with Chiral Ferrocene Ligands
Li-Xin Dai;Tao Tu;Shu-Li You;Wei-Ping Deng.
Accounts of Chemical Research (2003)
Transition-Metal-Catalyzed Asymmetric Allylic Dearomatization Reactions
Chun-Xiang Zhuo;Chao Zheng;Shu-Li You.
Accounts of Chemical Research (2014)
Transfer hydrogenation with Hantzsch esters and related organic hydride donors
Chao Zheng;Shu-Li You.
Chemical Society Reviews (2012)
Highly Enantioselective Friedel—Crafts Reaction of Indoles with Imines by a Chiral Phosphoric Acid.
Qiang Kang;Zhuo-An Zhao;Shu-Li You.
Journal of the American Chemical Society (2007)
Recent development of direct asymmetric functionalization of inert C–H bonds
Chao Zheng;Shu-Li You.
RSC Advances (2014)
Catalytic asymmetric dearomatization (CADA) reactions of phenol and aniline derivatives
Wen-Ting Wu;Liming Zhang;Shu-Li You.
Chemical Society Reviews (2016)
Recent developments in asymmetric transfer hydrogenation with Hantzsch esters: a biomimetic approach.
Chemistry-an Asian Journal (2007)
Highly regio- and enantioselective Pd-catalyzed allylic alkylation and amination of monosubstituted allylic acetates with novel ferrocene P,N-ligands.
Shu-Li You;Xia-Zhen Zhu;Yu-Mei Luo;Xue-Long Hou.
Journal of the American Chemical Society (2001)
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