Shinobu Itoh mostly deals with Copper, Photochemistry, Medicinal chemistry, Organic chemistry and Stereochemistry. His Copper research integrates issues from Tetrahedral molecular geometry and Polymer chemistry. The concepts of his Photochemistry study are interwoven with issues in Inorganic chemistry, Ion, Bond cleavage and Peroxide.
His Medicinal chemistry research is multidisciplinary, incorporating elements of Homolysis, Ligand, Toluene, Reactivity and Reaction mechanism. His work on Catalysis, Tyrosinase, Phenols and β diketiminate as part of general Organic chemistry study is frequently connected to Monomer dimer, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them. Shinobu Itoh combines subjects such as Pyridine, C h bond, Hydroxylation, Substrate and Redox with his study of Stereochemistry.
His primary areas of study are Medicinal chemistry, Stereochemistry, Copper, Ligand and Photochemistry. His work carried out in the field of Medicinal chemistry brings together such families of science as Hydroxylation, Adduct, Catalysis, Redox and Amine gas treating. He focuses mostly in the field of Stereochemistry, narrowing it down to topics relating to Active site and, in certain cases, Tyrosinase.
His Copper research includes elements of Inorganic chemistry, Reactive intermediate, Reactivity and Polymer chemistry. His Ligand research incorporates elements of Pyridine, Galactose oxidase, Nickel, Crystallography and Moiety. His Photochemistry study integrates concerns from other disciplines, such as Ion, Electron paramagnetic resonance and Bond cleavage.
His primary scientific interests are in Medicinal chemistry, Copper, Ligand, Catalysis and Reactivity. His studies in Medicinal chemistry integrate themes in fields like Tetrahydrofuran, Hydroxylation, Inorganic chemistry, Organic chemistry and Reaction mechanism. Shinobu Itoh interconnects Photochemistry, Tyrosinase, Stereochemistry, Reactive intermediate and Diamine in the investigation of issues within Copper.
The study incorporates disciplines such as Rhodium, Tris, Polymer chemistry and Nickel in addition to Ligand. Shinobu Itoh has included themes like Adduct and Cerium in his Catalysis study. The Reactivity study combines topics in areas such as Nanoscopic scale, Resonance, Bond cleavage, Electron paramagnetic resonance and Superoxide.
Copper, Photochemistry, Stereochemistry, Ligand and Catalysis are his primary areas of study. His Copper research is multidisciplinary, relying on both Reactive intermediate and Tyrosinase. The various areas that he examines in his Photochemistry study include Bond cleavage, Electron paramagnetic resonance, Reactivity, Redox and Peroxide.
His Stereochemistry research incorporates themes from Crystallography, Tetrabutylammonium hydroxide, Active site, Molecule and Coordination geometry. His Ligand research includes themes of Amination, Rhodium and Methanol. His Catalysis study combines topics in areas such as Carboxylate, Medicinal chemistry, Dioxygenase and Cerium.
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.
Monooxygenase Activity of Type 3 Copper Proteins
Shinobu Itoh;Shunichi Fukuzumi.
Accounts of Chemical Research (2007)
Selective One-Electron and Two-Electron Reduction of C60 with NADH and NAD Dimer Analogues via Photoinduced Electron Transfer
Shunichi Fukuzumi;Tomoyoshi Suenobu;Matthias Patz;Takeomi Hirasaka.
Journal of the American Chemical Society (1998)
Mononuclear copper active-oxygen complexes
Shinobu Itoh.
Current Opinion in Chemical Biology (2006)
Oxygenation of Phenols to Catechols by A (μ-η2:η2-Peroxo)dicopper(II) Complex: Mechanistic Insight into the Phenolase Activity of Tyrosinase
Shinobu Itoh;Hideyuki Kumei;Masayasu Taki;Shigenori Nagatomo.
Journal of the American Chemical Society (2001)
Oxidation Mechanism of Phenols by Dicopper−Dioxygen (Cu2/O2) Complexes
Takao Osako;Kei Ohkubo;Masayasu Taki;Yoshimitsu Tachi.
Journal of the American Chemical Society (2003)
Mononuclear Copper(II)−Superoxo Complexes that Mimic the Structure and Reactivity of the Active Centers of PHM and DβM
Atsushi Kunishita;Minoru Kubo;Hideki Sugimoto;Takashi Ogura.
Journal of the American Chemical Society (2009)
Aliphatic Hydroxylation by a Bis(μ-oxo)dicopper(III) Complex
Shinobu Itoh;Masayasu Taki;Hajime Nakao;Patrick L. Holland.
Angewandte Chemie (2000)
Fine-tuning of copper(I)-dioxygen reactivity by 2-(2-pyridyl)ethylamine bidentate ligands.
Masayasu Taki;Shinichi Teramae;Shigenori Nagatomo;Yoshimitsu Tachi.
Journal of the American Chemical Society (2002)
Copper chemistry of β-diketiminate ligands: Monomer/dimer equilibria and a new class of bis(μ-oxo)dicopper compounds
Douglas J. E. Spencer;Anne M. Reynolds;Patrick L. Holland;Brian A. Jazdzewski.
Inorganic Chemistry (2002)
NiII(TPA) as an efficient catalyst for alkane hydroxylation with m-CPBA
Takayuki Nagataki;Yoshimitsu Tachi;Shinobu Itoh.
Chemical Communications (2006)
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:
Ewha Womans University
University of Hyogo
Osaka University
The Graduate University for Advanced Studies, SOKENDAI
Osaka University
University of Minnesota
University of New Mexico
Kyushu University
Kyushu University
Johns Hopkins University
University of Illinois at Urbana-Champaign
City University of Hong Kong
Harvard University
Princeton University
Grenoble Alpes University
Stanford University
University of Maryland College of Agriculture and Natural Resources
University of Montreal
University of Strasbourg
Australian Museum
Goethe University Frankfurt
University of South Florida
National Institutes of Health
University of Amsterdam
Microsoft (United States)
Stanford University