2019 - Member of Academia Europaea
Xiaoming Feng mainly investigates Enantioselective synthesis, Organic chemistry, Catalysis, Combinatorial chemistry and Stereochemistry. His work carried out in the field of Enantioselective synthesis brings together such families of science as Medicinal chemistry, Lewis acids and bases, Trimethylsilyl cyanide, Aldimine and Nucleophile. Xiaoming Feng has included themes like Aza-Diels–Alder reaction and Enantiopure drug in his Medicinal chemistry study.
His work deals with themes such as Ketone, Reactivity and Alkyl, which intersect with Catalysis. His biological study deals with issues like Ligand, which deal with fields such as Stereoisomerism. His Michael reaction study integrates concerns from other disciplines, such as Bifunctional and Guanidine.
The scientist’s investigation covers issues in Catalysis, Enantioselective synthesis, Organic chemistry, Medicinal chemistry and Combinatorial chemistry. The various areas that Xiaoming Feng examines in his Catalysis study include Yield, Stereochemistry and Scandium. His Enantioselective synthesis course of study focuses on Michael reaction and Addition reaction.
All of his Organic chemistry and Aldol reaction, Titanium, Diels–Alder reaction, Friedel–Crafts reaction and Bifunctional investigations are sub-components of the entire Organic chemistry study. Xiaoming Feng regularly ties together related areas like Alkylation in his Friedel–Crafts reaction studies. His Medicinal chemistry research incorporates themes from Ligand, Ring, Lewis acids and bases and Nickel.
His primary areas of investigation include Catalysis, Enantioselective synthesis, Medicinal chemistry, Combinatorial chemistry and Cycloaddition. His Catalysis research entails a greater understanding of Organic chemistry. Xiaoming Feng has researched Enantioselective synthesis in several fields, including Bimetallic strip, Reaction conditions, Catalytic cycle, Stereochemistry and Optically active.
The various areas that Xiaoming Feng examines in his Stereochemistry study include Michael reaction and Desymmetrization. In Medicinal chemistry, he works on issues like Silylation, which are connected to Ketene. His work focuses on many connections between Combinatorial chemistry and other disciplines, such as Lewis acids and bases, that overlap with his field of interest in Intermolecular force.
His scientific interests lie mostly in Catalysis, Enantioselective synthesis, Combinatorial chemistry, Organic chemistry and Medicinal chemistry. His work deals with themes such as Yield and Optically active, which intersect with Catalysis. His research in Enantioselective synthesis intersects with topics in Bifunctional, Bimetallic strip, Guanidine, Reaction conditions and Stereochemistry.
His Stereochemistry research is multidisciplinary, relying on both Michael reaction and Desymmetrization. His studies in Combinatorial chemistry integrate themes in fields like Organocatalysis and Nucleophile. The Medicinal chemistry study combines topics in areas such as Scandium, Intramolecular force and Nickel.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Chiral N,N′-Dioxides: New Ligands and Organocatalysts for Catalytic Asymmetric Reactions
XiaoHua Liu;LiLi Lin;XiaoMing Feng.
Accounts of Chemical Research (2011)
Asymmetric Strecker Reactions
Jun Wang;Xiaohua Liu;Xiaoming Feng.
Chemical Reviews (2011)
Recent progress in enantioselective synthesis of C3-functionalized oxindoles: rare earth metals take action
Ke Shen;Xiaohua Liu;Lili Lin;Xiaoming Feng.
Chemical Science (2012)
Chiral N,N′-dioxide ligands: synthesis, coordination chemistry and asymmetric catalysis
Xiaohua Liu;Lili Lin;Xiaoming Feng.
Organic chemistry frontiers (2014)
Amide-based bifunctional organocatalysts in asymmetric reactions
Xiaohua Liu;Lili Lin;Xiaoming Feng.
Chemical Communications (2009)
A new copper(I)-tetrahydrosalen-catalyzed asymmetric Henry reaction and its extension to the synthesis of (S)-norphenylephrine.
Yan Xiong;Fei Wang;Xiao Huang;Yuehong Wen.
Chemistry: A European Journal (2007)
Asymmetric three-component inverse electron-demand aza-Diels-Alder reaction: efficient synthesis of ring-fused tetrahydroquinolines.
M. Xie;X. Chen;Y. Zhu;B. Gao.
Angewandte Chemie (2010)
Catalytic Asymmetric Cyanosilylation of Ketones by a Chiral Amino Acid Salt
Xiaohua Liu;Bo Qin;Xin Zhou;Bin He.
Journal of the American Chemical Society (2005)
Highly Enantioselective Henry (Nitroaldol) Reaction of Aldehydes and α-Ketoesters Catalyzed by N,N‘-Dioxide-Copper(I) Complexes
Bo Qin;Xiao Xiao;Xiaohua Liu;Jinglun Huang.
Journal of Organic Chemistry (2007)
Asymmetric Cycloaddition and Cyclization Reactions Catalyzed by Chiral N,N′-Dioxide–Metal Complexes
Xiaohua Liu;Haifeng Zheng;Yong Xia;Lili Lin.
Accounts of Chemical Research (2017)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
Sichuan University
Sichuan University
Sichuan University
Chinese Academy of Sciences
University of Hawaii at Manoa
Colorado State University
Tsinghua University
Nanyang Technological University
Sun Yat-sen University
Chinese Academy of Sciences
Imperial College London
Chalmers University of Technology
Aix-Marseille University
Peking University
University of Oxford
University of Missouri–St. Louis
Charles University
University of South Florida
University of Kansas
Max Planck Society
Centre national de la recherche scientifique, CNRS
United States Geological Survey
Cheng Shiu University
Brown University
The University of Texas Health Science Center at San Antonio
University of Cambridge