His primary areas of investigation include Enantioselective synthesis, Catalysis, Organic chemistry, Medicinal chemistry and Stereochemistry. His Enantioselective synthesis research integrates issues from Stereoisomerism, Insertion reaction, Hydrogen bond, Copper and Carbenoid. His research investigates the connection between Hydrogen bond and topics such as Combinatorial chemistry that intersect with problems in Green chemistry and Reaction conditions.
His work on Olefin fiber as part of his general Catalysis study is frequently connected to Phosphoramidite, thereby bridging the divide between different branches of science. Organic chemistry is a component of his Iridium, Allylic rearrangement, Transition metal, Asymmetric hydrogenation and Noyori asymmetric hydrogenation studies. In his research on the topic of Photochemistry, Reactivity, Organic synthesis and Carbene is strongly related with Heteroatom.
His primary scientific interests are in Catalysis, Enantioselective synthesis, Organic chemistry, Medicinal chemistry and Combinatorial chemistry. In the field of Catalysis, his study on Iridium, Asymmetric hydrogenation and Allylic rearrangement overlaps with subjects such as Phosphoramidite. His Enantioselective synthesis study combines topics from a wide range of disciplines, such as Copper catalyzed, Copper, Nickel, Insertion reaction and Stereochemistry.
His study on Noyori asymmetric hydrogenation, Phosphine and Yield is often connected to Surface modification as part of broader study in Organic chemistry. His study looks at the relationship between Medicinal chemistry and topics such as Hydrogen bond, which overlap with Reaction rate. In Combinatorial chemistry, he works on issues like Intramolecular force, which are connected to Cyclopropanation.
His primary areas of study are Catalysis, Enantioselective synthesis, Combinatorial chemistry, Medicinal chemistry and Organic chemistry. The Catalysis study combines topics in areas such as Intramolecular force and Polymer chemistry. His Enantioselective synthesis study combines topics in areas such as Enol, Stereochemistry, Carbene and Rhodium.
His research in Combinatorial chemistry intersects with topics in Reagent, Regioselectivity, Reaction conditions, Organic synthesis and Total synthesis. The concepts of his Medicinal chemistry study are interwoven with issues in Friedel–Crafts reaction and Insertion reaction. His study in the field of Copper also crosses realms of Oxidative phosphorylation and Surface modification.
Shou-Fei Zhu spends much of his time researching Catalysis, Enantioselective synthesis, Carbene, Combinatorial chemistry and Organic chemistry. His work carried out in the field of Catalysis brings together such families of science as Intramolecular force and Ligand. His Intramolecular force research is multidisciplinary, relying on both Yield, Cyclopropanation and Copper.
His Enantioselective synthesis research includes elements of Indole test, Stereochemistry, Rhodium and Medicinal chemistry. Shou-Fei Zhu interconnects Insertion reaction, Diazo, Borane, Organic synthesis and Hydrogen bond in the investigation of issues within Carbene. Asymmetric hydrogenation and Iridium are the primary areas of interest in his Organic chemistry study.
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.
Transition Metal-Catalyzed Enantioselective Hydrogenation of Enamines and Imines
Jian-Hua Xie;Shou-Fei Zhu;Qi-Lin Zhou.
Chemical Reviews (2011)
Transition-metal-catalyzed enantioselective heteroatom-hydrogen bond insertion reactions.
Shou-Fei Zhu;Qi-Lin Zhou.
Accounts of Chemical Research (2012)
Chiral Brønsted Acid Catalyzed Enantioselective Friedel–Crafts Reaction of Indoles and α-Aryl Enamides: Construction of Quaternary Carbon Atoms†
Yi-Xia Jia;Jun Zhong;Shou-Fei Zhu;Can-Ming Zhang.
Angewandte Chemie (2007)
Asymmetric NH Insertion Reaction Cooperatively Catalyzed by Rhodium and Chiral Spiro Phosphoric Acids
Bin Xu;Shou-Fei Zhu;Xiu-Lan Xie;Jun-Jie Shen.
Angewandte Chemie (2011)
Well-defined chiral spiro iridium/phosphine-oxazoline cationic complexes for highly enantioselective hydrogenation of imines at ambient pressure.
Shou-Fei Zhu;Jian-Bo Xie;Yong-Zhen Zhang;Shen Li.
Journal of the American Chemical Society (2006)
Enantioselective iron-catalysed O–H bond insertions
Shou-Fei Zhu;Yan Cai;Hong-Xiang Mao;Jian-Hua Xie.
Nature Chemistry (2010)
Highly enantioselective insertion of carbenoids into O-H bonds of phenols: an efficient approach to chiral alpha-aryloxycarboxylic esters.
Chao Chen;Shou-Fei Zhu;Bin Liu;Li-Xin Wang.
Journal of the American Chemical Society (2007)
Highly Enantioselective Insertion of Carbenoids into N−H Bonds Catalyzed by Copper Complexes of Chiral Spiro Bisoxazolines
Bin Liu;Shou-Fei Zhu;Wei Zhang;Chao Chen.
Journal of the American Chemical Society (2007)
Recent advances in transition metal-catalyzed enantioselective hydrogenation of unprotected enamines
Jian-Hua Xie;Shou-Fei Zhu;Qi-Lin Zhou.
Chemical Society Reviews (2012)
Iridium-Catalyzed Asymmetric Hydrogenation of Unsaturated Carboxylic Acids.
Shou-Fei Zhu;Qi-Lin Zhou.
Accounts of Chemical Research (2017)
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