Xumu Zhang mainly investigates Catalysis, Organic chemistry, Enantioselective synthesis, Asymmetric hydrogenation and Medicinal chemistry. The study incorporates disciplines such as Combinatorial chemistry and Ligand in addition to Catalysis. His biological study deals with issues like Stereochemistry, which deal with fields such as Amino acid.
His biological study spans a wide range of topics, including Noyori asymmetric hydrogenation, Ruthenium, Imine, Phosphorus and Enantiopure drug. While the research belongs to areas of Medicinal chemistry, Xumu Zhang spends his time largely on the problem of Cycloaddition, intersecting his research to questions surrounding Coupling reaction. His study in Rhodium is interdisciplinary in nature, drawing from both Cycloisomerization and Enantiomer.
His main research concerns Catalysis, Organic chemistry, Enantioselective synthesis, Asymmetric hydrogenation and Ligand. His research in Catalysis tackles topics such as Medicinal chemistry which are related to areas like Denticity. His study in Organic chemistry concentrates on Noyori asymmetric hydrogenation, Hydroformylation, Phosphine, Aryl and Regioselectivity.
The Enantioselective synthesis study which covers Stereochemistry that intersects with Stereocenter. His Asymmetric hydrogenation research integrates issues from Thiourea, Nickel, Ruthenium, Substrate and Organic synthesis. His Ligand research incorporates elements of Selectivity, Reactivity and Enantiomer.
The scientist’s investigation covers issues in Catalysis, Asymmetric hydrogenation, Organic chemistry, Enantioselective synthesis and Combinatorial chemistry. His Catalysis research is multidisciplinary, relying on both Yield and Medicinal chemistry. Xumu Zhang interconnects Thiourea, Nickel, Ligand, Stereochemistry and Noyori asymmetric hydrogenation in the investigation of issues within Asymmetric hydrogenation.
His work on Phosphine, Catalytic hydrogenation, Allylic rearrangement and Reaction mechanism as part of general Organic chemistry study is frequently connected to Ton, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them. The various areas that Xumu Zhang examines in his Enantioselective synthesis study include Cycloisomerization and Moiety. His Combinatorial chemistry study combines topics in areas such as Denticity, Ruthenium, Reductive amination, Chirality and Phosphine oxide.
His primary areas of investigation include Catalysis, Asymmetric hydrogenation, Organic chemistry, Enantioselective synthesis and Combinatorial chemistry. His research integrates issues of Yield and Thiourea in his study of Catalysis. The Asymmetric hydrogenation study combines topics in areas such as Enantiomeric excess, Medicinal chemistry, Ligand, Organic synthesis and Enantiomer.
His Ligand research is multidisciplinary, incorporating elements of Cobalt and Stereochemistry. His Enantioselective synthesis study frequently draws parallels with other fields, such as Reactivity. His Combinatorial chemistry study integrates concerns from other disciplines, such as Reductive amination, Primary, Phosphine oxide, Selectivity and Intramolecular force.
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New Chiral Phosphorus Ligands for Enantioselective Hydrogenation
Wenjun Tang;Xumu Zhang.
Chemical Reviews (2003)
Regioselective and enantioselective epoxidation catalyzed by metalloporphyrins
James P. Collman;Xumu Zhang;Virgil J. Lee;Erich S. Uffelman.
Science (1993)
Highly Enantioselective Ag(I)-Catalyzed [3 + 2] Cycloaddition of Azomethine Ylides
James M. Longmire;Bin Wang;Xumu Zhang.
Journal of the American Chemical Society (2002)
Asymmetric [3 + 2] Cycloaddition of 2,3-Butadienoates with Electron-Deficient Olefins Catalyzed by Novel Chiral 2,5-Dialkyl-7-phenyl-7- phosphabicyclo[2.2.1]heptanes
Guoxin Zhu;Zhaogen Chen;Qiongzhong Jiang;Dengming Xiao.
Journal of the American Chemical Society (1997)
Developing chiral ligands for asymmetric hydrogenation.
Weicheng Zhang;Yongxiang Chi;Xumu Zhang.
Accounts of Chemical Research (2007)
A Chiral 1,2‐Bisphospholane Ligand with a Novel Structural Motif: Applications in Highly Enantioselective Rh‐Catalyzed Hydrogenations
Wenjun Tang;Xumu Zhang.
Angewandte Chemie (2002)
Synthesis of chiral bisphosphines with tunable bite angles and their applications in asymmetric hydrogenation of beta-ketoesters.
Zhaoguo Zhang;Hu Qian;James Longmire;Xumu Zhang.
Journal of Organic Chemistry (2000)
Chiral Bronsted acid catalyzed asymmetric Baeyer-Villiger reaction of 3-substituted cyclobutanones by using aqueous H2O2
Senmiao Xu;Zheng Wang;Xue Zhang;Xumu Zhang.
Angewandte Chemie (2008)
Synthesis and X-ray Crystal Structures of Palladium(II) and Platinum(II) Complexes of the PCP-Type Chiral Tridentate Ligand (1R,1‘R)-1,3-Bis[1-(diphenylphosphino)ethyl]benzene. Use in the Asymmetric Aldol Reaction of Methyl Isocyanoacetate and Aldehydes
James M. Longmire;Xumu Zhang;Maoyu Shang.
Organometallics (1998)
A Functional Model Related to Cytochrome c Oxidase and Its Electrocatalytic Four-Electron Reduction of O2
James P. Collman;Lei Fu;Paul C. Herrmann;Xumu Zhang.
Science (1997)
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