D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Chemistry D-index 89 Citations 26,458 463 World Ranking 914 National Ranking 118

Overview

What is he best known for?

The fields of study he is best known for:

  • Catalysis
  • Organic chemistry
  • Alkene

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 most cited work include:

  • New Chiral Phosphorus Ligands for Enantioselective Hydrogenation (1557 citations)
  • Regioselective and enantioselective epoxidation catalyzed by metalloporphyrins (323 citations)
  • Highly Enantioselective Ag(I)-Catalyzed [3 + 2] Cycloaddition of Azomethine Ylides (270 citations)

What are the main themes of his work throughout his whole career to date?

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.

He most often published in these fields:

  • Catalysis (88.35%)
  • Organic chemistry (56.93%)
  • Enantioselective synthesis (55.60%)

What were the highlights of his more recent work (between 2015-2021)?

  • Catalysis (88.35%)
  • Asymmetric hydrogenation (57.37%)
  • Organic chemistry (56.93%)

In recent papers he was focusing on the following fields of study:

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.

Between 2015 and 2021, his most popular works were:

  • Strong Brønsted acid promoted asymmetric hydrogenation of isoquinolines and quinolines catalyzed by a Rh–thiourea chiral phosphine complex via anion binding (69 citations)
  • Asymmetric Synthesis of Chiral Primary Amines by Ruthenium-Catalyzed Direct Reductive Amination of Alkyl Aryl Ketones with Ammonium Salts and Molecular H2 (56 citations)
  • Iridium Catalysts with f-Amphox Ligands: Asymmetric Hydrogenation of Simple Ketones. (53 citations)

In his most recent research, the most cited papers focused on:

  • Catalysis
  • Organic chemistry
  • Alkene

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.

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.

Best Publications

New Chiral Phosphorus Ligands for Enantioselective Hydrogenation

Wenjun Tang;Xumu Zhang.
Chemical Reviews (2003)

2221 Citations

Regioselective and enantioselective epoxidation catalyzed by metalloporphyrins

James P. Collman;Xumu Zhang;Virgil J. Lee;Erich S. Uffelman.
Science (1993)

499 Citations

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)

408 Citations

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)

393 Citations

Developing chiral ligands for asymmetric hydrogenation.

Weicheng Zhang;Yongxiang Chi;Xumu Zhang.
Accounts of Chemical Research (2007)

338 Citations

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)

306 Citations

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)

256 Citations

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)

251 Citations

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)

244 Citations

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)

237 Citations

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