World's Best Scientists 2026 revealed!
Toshifumi Dohi

Toshifumi Dohi

D-Index & Metrics

Chemistry

D-Index
47
Citations
9866
World Ranking
15523
National Ranking
1213

Overview

Toshifumi Dohi is affiliated with Ritsumeikan University in Japan and works primarily in the field of chemistry. Their research focuses largely on organic chemistry, with significant contributions to the study of oxidative organic chemistry reactions and catalytic processes.

The scientist's work covers several specialized subfields including:

  • Organic Chemistry
  • Inorganic Chemistry
  • Pharmaceutical Science
  • Molecular Biology
  • Pharmacology

Dohi's research includes notable topics such as:

  • Oxidative Organic Chemistry Reactions
  • Catalytic C-H Functionalization Methods
  • Synthesis and Catalytic Reactions
  • Chemical Synthesis and Reactions
  • Vanadium and Halogenation Chemistry
  • Sulfur-Based Synthesis Techniques
  • Fluorine in Organic Chemistry

Recent publications reflect a focus on hypervalent iodine reagents and their role in organic synthesis and catalytic chemistry. Selected papers include:

  • Palladium-Catalyzed Organic Reactions Involving Hypervalent Iodine Reagents, 2022, Molecules
  • Non-Palladium-Catalyzed Oxidative Coupling Reactions Using Hypervalent Iodine Reagents, 2022, Frontiers in Chemistry
  • Asymmetric Direct/Stepwise Dearomatization Reactions Involving Hypervalent Iodine Reagents, 2021, Chemistry - An Asian Journal
  • Iodine(iii) Reagents for Oxidative Aromatic Halogenation, 2022, Organic & Biomolecular Chemistry
  • Halogen-Induced Controllable Cyclizations as Diverse Heterocycle Synthetic Strategy, 2020, Molecules

Dohi has frequently collaborated with a number of researchers in the field, including:

  • Kotaro Kikushima
  • Ravi Kumar
  • Naoko Takenaga
  • Fateh V. Singh
  • Yasuyuki Kita

The scientist's work is often published in venues such as:

  • Frontiers in Chemistry
  • Molecules
  • Chemistry - An Asian Journal
  • Organic Letters
  • Synthesis

Best Publications

  • Hypervalent iodine reagents as a new entrance to organocatalysts

    Toshifumi Dohi;Yasuyuki Kita

  • A chiral hypervalent iodine(III) reagent for enantioselective dearomatization of phenols

    Toshifumi Dohi;Akinobu Maruyama;Naoko Takenaga;Kento Senami

  • Versatile hypervalent-iodine(III)-catalyzed oxidations with m-chloroperbenzoic acid as a cooxidant.

    Toshifumi Dohi;Akinobu Maruyama;Misaki Yoshimura;Koji Morimoto

  • Metal-Free Oxidative Cross-Coupling of Unfunctionalized Aromatic Compounds

    Yasuyuki Kita;Koji Morimoto;Motoki Ito;Chieko Ogawa

  • Asymmetric dearomatizing spirolactonization of naphthols catalyzed by spirobiindane-based chiral hypervalent iodine species.

    Toshifumi Dohi;Naoko Takenaga;Tomofumi Nakae;Yosuke Toyoda

  • Fluoroalcohols: versatile solvents in hypervalent iodine chemistry and syntheses of diaryliodonium(III) salts

    Toshifumi Dohi;Nobutaka Yamaoka;Yasuyuki Kita

  • Hypervalent iodine(III): selective and efficient single-electron-transfer (SET) oxidizing agent

    Toshifumi Dohi;Toshifumi Dohi;Motoki Ito;Nobutaka Yamaoka;Koji Morimoto

  • Oxidative Cross‐Coupling of Arenes Induced by Single‐Electron Transfer Leading to Biaryls by Use of Organoiodine(III) Oxidants

    Toshifumi Dohi;Motoki Ito;Koji Morimoto;Minako Iwata

  • Unusual ipso Substitution of Diaryliodonium Bromides Initiated by a Single‐Electron‐Transfer Oxidizing Process

    Toshifumi Dohi;Motoki Ito;Nobutaka Yamaoka;Koji Morimoto

  • First hypervalent iodine(III)-catalyzed C-N bond forming reaction: catalytic spirocyclization of amides to N-fused spirolactams.

    Toshifumi Dohi;Akinobu Maruyama;Yutaka Minamitsuji;Naoko Takenaga

  • Iodoarene-catalyzed fluorination and aminofluorination by an Ar-I/HF·pyridine/mCPBA system

    Satoru Suzuki;Tomohiro Kamo;Kazunobu Fukushi;Takaaki Hiramatsu

  • A new H2O2/acid anhydride system for the iodoarene-catalyzed C-C bond-forming reactions of phenols.

    Toshifumi Dohi;Yutaka Minamitsuji;Akinobu Maruyama;Satoshi Hirose

  • Organocatalytic C-H/C-H′ Cross-Biaryl Coupling: C-Selective Arylation of Sulfonanilides with Aromatic Hydrocarbons.

    Motoki Ito;Hiroko Kubo;Itsuki Itani;Koji Morimoto

  • Direct synthesis of bipyrroles using phenyliodine bis(trifluoroacetate) with bromotrimethylsilane.

    Toshifumi Dohi;Koji Morimoto;and Akinobu Maruyama;Yasuyuki Kita

  • Clean and Efficient Benzylic C−H Oxidation in Water Using a Hypervalent Iodine Reagent: Activation of Polymeric Iodosobenzene with KBr in the Presence of Montmorillonite-K10

    Toshifumi Dohi;Naoko Takenaga;Akihiro Goto;Hiromichi Fujioka

  • Pioneering Metal-Free Oxidative Coupling Strategy of Aromatic Compounds Using Hypervalent Iodine Reagents

    Yasuyuki Kita;Toshifumi Dohi

  • Versatile direct dehydrative approach for diaryliodonium(III) salts in fluoroalcohol media

    Toshifumi Dohi;Motoki Ito;Koji Morimoto;Yutaka Minamitsuji

  • Direct lactone formation by using hypervalent iodine(III) reagents with KBr via selective C-H abstraction protocol.

    Toshifumi Dohi;Naoko Takenaga;Akihiro Goto;and Akinobu Maruyama

  • Direct Cyanation of Heteroaromatic Compounds Mediated by Hypervalent Iodine(III) Reagents: In Situ Generation of PhI(III)−CN Species and Their Cyano Transfer

    Toshifumi Dohi;Koji Morimoto;Naoko Takenaga;Akihiro Goto

  • Metal-free oxidative para cross-coupling of phenols.

    Koji Morimoto;Kazuma Sakamoto;Yusuke Ohnishi;Takeshi Miyamoto

Frequent Co-Authors

Yasuyuki Kita
Yasuyuki Kita Ritsumeikan University
Motoo Shiro
Motoo Shiro Nagoya Institute of Technology
Shuji Akai
Shuji Akai Osaka University
Hironao Sajiki
Hironao Sajiki Gifu Pharmaceutical University
Yasunari Monguchi
Yasunari Monguchi Gifu Pharmaceutical University
Naoto Chatani
Naoto Chatani Osaka University
Masamichi Ogasawara
Masamichi Ogasawara University of Tokushima
Shinji Murai
Shinji Murai Osaka University
Norio Shibata
Norio Shibata Nagoya Institute of Technology
Tomofusa Tsuchiya
Tomofusa Tsuchiya Okayama University

If you think any of the details on this page are incorrect, let us know.

Report an issue

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:

Related Online Degrees & Career Pathways

Studying Chemistry in the USA can open diverse career pathways, including specialized fields like forensic science. For students interested in the intersection of science and criminal justice, pursuing a master's in forensic psychology online offers an accessible way to deepen expertise from anywhere.

Understanding the forensic career paths is crucial for Chemistry graduates aiming to work in crime labs or law enforcement agencies. These roles often require knowledge of both chemical principles and legal procedures, blending scientific analysis with investigative skills.

Cost considerations are important when selecting a degree program. Resources detailing how much is a criminal justice degree can help prospective students budget effectively for their education, especially when choosing between online and on-campus options.

For those just starting, exploring the best online associates in criminal justice provides foundational knowledge and can serve as a stepping stone toward more advanced studies or career opportunities linked to Chemistry and forensic sciences.

Best Scientists Citing Toshifumi Dohi

Trending Scientists

Recently Published Articles