Hironao Sajiki

Professor

Gifu Pharmaceutical University

Japan

Research Interests

Explore related searches

Professors in Japan Professors in Organic Chemistry Organic Chemistry professors in Japan

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

About

Hironao Sajiki is a Professor at Gifu Pharmaceutical University in Japan. His research focuses on catalysis, particularly in the development of robust palladium catalysts and their application in continuous-flow systems. Recent publications include studies on carbon-carbon bond formation, synthesis of isoquinolones, and mechanisms of catalysis involving various metal catalysts.

Articles (23)

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2025

Year:

2024

Year:

2024

Year:

2024

Year:

2023

Year:

2023

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Collaborators (7)

Takashi Ikawa

Associate Professor

Gifu Pharmaceutical University

JAPAN

View details

Makoto Makishima

Nihon University School of Medicine

JAPAN

View details

Kwihwan Kobayashi

National Institute of Advanced Industrial Science and Technology

JAPAN

View details

Takakazu Nakabayashi

Tohoku University

JAPAN

View details

Tsuyoshi Yamada

Associate Professor

Gifu University

JAPAN

View details

Shinji Kajimoto

Associate Professor

Tohoku University

JAPAN

View details

Taro Matsumoto

Nihon University School of Medicine

JAPAN

View details

ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.

Hironao Sajiki

Research Interests

Explore related searches

Contact this professor

About

Articles (23)

Cover Feature: Durable Heterogeneous Pd‐PNP Pincer Complex for CarbonCarbon Bond Formation in Continuous‐Flow Systems (ChemSusChem 19/2025)

Durable Heterogeneous Pd‐PNP Pincer Complex for CarbonCarbon Bond Formation in Continuous‐Flow Systems

Silver-Catalyzed Synthesis of Isoquinolones via Oxazole Ring Opening

Cover Feature: Stable and Versatile Pd Precursors for the Preparation of Robust Pd Catalysts Under Continuous‐Flow (ChemSusChem 4/2025)

Stable and Versatile Pd Precursors for the Preparation of Robust Pd Catalysts Under Continuous‐Flow

Development of site- and stereoselective continuous flow deuterium labelling method for carbohydrates using high dispersion effect towards Ru/C of hydrogen flow

Electrochemically assisted deprotection of acetals, ketals, and dithioacetals under neutral conditions

Synthesis of cyclic carbonates via silver-catalysed fixation of CO2 to propargyl alcohols under mechanochemical conditions

Theoretical analysis of the reaction mechanism of D2 gas generation using a Pd/C catalyst

Synthesis of Functionalized Cyclic Ethers via Gold‐Catalyzed Cyclization and Rearrangement

Pt/CB-Catalyzed Chemoselective Hydrogenation Using In Situ-Generated Hydrogen by Microwave-Mediated Dehydrogenation of Methylcyclohexane under Continuous-Flow Conditions

Front Cover Picture: Gold‐Catalyzed Synthesis of Ortho‐Quinone Methide Analogues as Reactive Synthetic Precursors (Adv. Synth. Catal. 10/2024)

Gold‐Catalyzed Synthesis of Ortho‐Quinone Methide Analogues as Reactive Synthetic Precursors

Multiple deuteration of triphenylphosphine and live-cell Raman imaging of deuterium-incorporated Mito-Q

Syntheses of 25-Adamantyl-25-alkyl-2-methylidene-1α,25-dihydroxyvitamin D3 Derivatives with Structure–Function Studies of Antagonistic and Agonistic Active Vitamin D Analogs

Highly Selective Synthesis of cis‐2,2,4,4‐Tetramethylcyclobutane‐1,3‐diol via Solvent‐Free Hydrogenation and Isomerization

Aryl Boronic Esters Are Stable on Silica Gel and Reactive under Suzuki–Miyaura Coupling Conditions

Development of Silicon Carbide-Supported Palladium Catalysts and Their Application as Semihydrogenation Catalysts for Alkynes under Batch- and Continuous-Flow Conditions

Cover Feature: Highly Selective Hydrogenative Conversion of Nitriles into Tertiary, Secondary, and Primary Amines under Flow Reaction Conditions (ChemSusChem 2/2022)

Highly Selective Hydrogenative Conversion of Nitriles into Tertiary, Secondary, and Primary Amines under Flow Reaction Conditions

Multicomponent double Mannich alkylamination involving C(sp2)–H and benzylic C(sp3)–H bonds

Heavy water recycling for producing deuterium compounds

Oxidative two-way regiocontrolled coupling of 3-methoxycarbonylcatechol and indoles to arylindoles

Collaborators (7)

Takashi Ikawa

Makoto Makishima

Kwihwan Kobayashi

Takakazu Nakabayashi

Tsuyoshi Yamada

Shinji Kajimoto

Taro Matsumoto

Make your next move.