His primary areas of investigation include Catalysis, Enantioselective synthesis, Organic chemistry, Asymmetric hydrogenation and Medicinal chemistry. His Catalysis research incorporates themes from Intramolecular force and Stereochemistry. Qi-Lin Zhou has researched Enantioselective synthesis in several fields, including Combinatorial chemistry, Carbenoid, Ligand and Copper.
In his research, Phosphine and Group is intimately related to Polymer chemistry, which falls under the overarching field of Organic chemistry. His work carried out in the field of Asymmetric hydrogenation brings together such families of science as Noyori asymmetric hydrogenation, Ruthenium, Kinetic resolution and BINAP. Qi-Lin Zhou works mostly in the field of Medicinal chemistry, limiting it down to concerns involving Intermolecular force and, occasionally, Pentane, Cyclopropanation, Solvent effects and Aniline.
Qi-Lin Zhou mainly investigates Catalysis, Enantioselective synthesis, Organic chemistry, Asymmetric hydrogenation and Medicinal chemistry. His Iridium study in the realm of Catalysis connects with subjects such as Phosphoramidite. His Enantioselective synthesis study also includes fields such as
His research integrates issues of Kinetic resolution, Ruthenium, Group, Optically active and Total synthesis in his study of Asymmetric hydrogenation. His Medicinal chemistry research incorporates elements of Alkylation, Insertion reaction, Hydrogen bond, Enantiomer and Carbenoid. Qi-Lin Zhou interconnects Chiral ligand and Nickel in the investigation of issues within Combinatorial chemistry.
The scientist’s investigation covers issues in Catalysis, Enantioselective synthesis, Organic chemistry, Combinatorial chemistry and Asymmetric hydrogenation. His studies in Catalysis integrate themes in fields like Yield, Medicinal chemistry and Nickel. His Enantioselective synthesis study integrates concerns from other disciplines, such as Ligand, Intramolecular force, Stereochemistry and Carbene.
His work on Formic acid, Phosphine, Catalytic hydrogenation and Enantiomeric excess as part of his general Organic chemistry study is frequently connected to Oxidative phosphorylation, thereby bridging the divide between different branches of science. His work in Combinatorial chemistry addresses issues such as Reaction rate, which are connected to fields such as Hydrogen bond. His Asymmetric hydrogenation research integrates issues from Ketone, Kinetic resolution, Optically active and Reaction conditions.
Qi-Lin Zhou mainly focuses on Catalysis, Enantioselective synthesis, Organic chemistry, Combinatorial chemistry and Stereochemistry. His Catalysis research is multidisciplinary, incorporating elements of Yield and Nickel. His studies deal with areas such as Ligand, Carbene and Phosphine as well as Enantioselective synthesis.
His work in the fields of Organic chemistry, such as Formic acid, Ruthenium, Homogeneous catalysis and Amide, intersects with other areas such as Acrylic acid. In his research on the topic of Combinatorial chemistry, Benzene and Iron catalyzed is strongly related with Aryl. His Iridium study incorporates themes from Noyori asymmetric hydrogenation and Alkyl.
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 Diphosphine and Monodentate Phosphorus Ligands on a Spiro Scaffold for Transition-Metal-Catalyzed Asymmetric Reactions
Jian-Hua Xie;Qi-Lin Zhou.
Accounts of Chemical Research (2008)
Synthesis of spiro diphosphines and their application in asymmetric hydrogenation of ketones.
Jian-Hua Xie;Li-Xin Wang;Yu Fu;Shuo-Fei Zhu.
Journal of the American Chemical Society (2003)
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)
Asymmetric Friedel−Crafts Alkylations of Indoles with Nitroalkenes Catalyzed by Zn(II)−Bisoxazoline Complexes
Yi-Xia Jia;Shuo-Fei Zhu;Yun Yang;Qi-Lin Zhou.
Journal of Organic Chemistry (2006)
Monodentate chiral spiro phosphoramidites: efficient ligands for rhodium-catalyzed enantioselective hydrogenation of enamides.
Ai-Guo Hu;Yu Fu;Jian-Hua Xie;Hai Zhou.
Angewandte Chemie (2002)
Enantioselective iron-catalysed O–H bond insertions
Shou-Fei Zhu;Yan Cai;Hong-Xiang Mao;Jian-Hua Xie.
Nature Chemistry (2010)
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