Keisuke Nishikawa

Assistant Professor

Osaka Daigaku

Japan

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About

Keisuke Nishikawa is an Assistant Professor at Osaka Shiritsu Daigaku in Japan. His research focuses on the total synthesis and biological activity of natural products, particularly those derived from marine sources and plants. Recent publications include work on the asymmetric total synthesis of isolinearol and studies on halogenated cyclic monoterpenoids with anti-biofouling activity.

Articles (12)

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2025

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2025

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2024

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2024

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2023

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2023

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2023

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2022

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2022

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2022

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2021

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2021

Collaborators (2)

Yoshiki Morimoto

Osaka University

JAPAN

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Takahiro Ishii

Associate Professor

University of the Ryukyus

JAPAN

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Keisuke Nishikawa

Research Interests

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Articles (12)

Asymmetric Total Synthesis of Isolinearol Using Low-Valence Titanium and Evaluation of Its Inhibitory Activity against Mussel Byssal Thread Formation

Isolation and structural determination of natural products bearing tetrahydrogenated isoprenoid side-chains at their ω-termini

Halogenated Cyclic Monoterpenoids with Anti‐Biofouling Activity from the Okinawan Red Marine Algae Portieria Hornemannii

Divergent Nine-Step Syntheses of Perhydrohistrionicotoxin Analogs and Their Inhibition Activity Toward Chicken α4β2-Neuronal Nicotinic Acetylcholine Receptors

Front Cover: Two New Eremophilane‐Type Sesquiterpenoids from Japanese Liverwort Bazzania japonica (Chem. Biodiversity 4/2023)

Two New Eremophilane‐Type Sesquiterpenoids from Japanese Liverwort Bazzania japonica

Establishment of “Ring-Size-Divergent” Synthetic Strategy: Divergent Synthesis, Stereochemical Assignments, and Biological Activity Studies of Nerolidol-Type Sesquiterpenoids and Feroniellins

Asymmetric Total Synthesis of Toxicodenane A by Samarium-Iodide-Induced Barbier-Type Cyclization and Its Cell-Protective Effect against Lipotoxicity

Asymmetric Total Syntheses, Stereostructures, and Cytotoxicities of Marine Bromotriterpenoids Aplysiol B (Laurenmariannol) and Saiyacenol A

Front Cover: Asymmetric Total Syntheses, Stereostructures, and Cytotoxicities of Marine Bromotriterpenoids Aplysiol B (Laurenmariannol) and Saiyacenol A (Chem. Asian J. 1/2022)

Establishing a “Ring‐Size‐Divergent” Synthetic Strategy: Synthesis, Structural Revision, and Absolute Configuration of Feroniellins

One‐Step Synthesis of the 1‐Azaspiro[5.5]undecane Skeleton Characteristic of Histrionicotoxin Alkaloids from Linear Substrates via Hg(OTf)2‐Catalyzed Cycloisomerization

Collaborators (2)

Yoshiki Morimoto

Takahiro Ishii

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