Hideo Kigoshi

Professor

University of Tsukuba

Japan

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About

Hideo Kigoshi is a Professor at the University of Tsukuba, Japan. His research primarily focuses on synthetic chemistry and the biological evaluation of natural products, as demonstrated in his recent articles on cytotoxic macrolides, spiroacetals, and various marine compounds. He has contributed significantly to the fields of total synthesis and structure-activity relationship studies, advancing the understanding of complex organic molecules.

Articles (21)

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2024

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2022

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2022

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2021

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2021

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ETH Zürich

SWITZERLAND

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Hideo Kigoshi

Research Interests

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About

Articles (21)

Concise total synthesis of (−)-berkelic acid <i>via</i> regioselective spiroacetal/pyran formation

Development of the “Molecular Glue” Using Hybridization of Natural Products,天然物ハイブリッド化による『分子のり』の創出

Skin- and airway-deliverable TRPA1 inhibitor

Structure revision of lagunamide C to odoamide by total synthesis and biological evaluation

Structure–Activity Relationship Studies on Scytophycin B, a Spiro-Epoxide-Containing Cytotoxic Macrolide

Total Synthesis of Aplysiasecosterols A and B, Two Marine 9,11-Secosteroids

Correction to “Isolation and Synthesis of Azuriaplysins A and B, Bromoditerpenes with an α-Methylene Carbonyl from the Sea Hare Aplysia kurodai”

Concise Total Synthesis and Biological Evaluation of Pargamicin A and its Diastereomer, Piperazic Acid‐containing Cyclopeptides

Concise total synthesis and structure revision of metacridamides A and B

Synthesis and Biological Evaluation of Siladenoserinol A Analogs Possessing a Diastereomeric 6,8-Dioxabicyclo[3.2.1]octane Skeleton

Toward the total synthesis of scytophycins: Synthesis of the C7–C21 fragments of scytophycins A, B, and C

Structure–activity relationship studies on an antitumor marine macrolide using aplyronine a–swinholide A hybrid

"Isolation and Synthesis of Azuriaplysins A and B, Bromoditerpenes with an a-Methylene Carbonyl from the Sea Hare Aplysia kurodai"(vol 85, pg 2082, 2022)

Bioinspired Total Synthesis and Structure-Activity Relationship Studies on Aplaminal

Isolation and Synthesis of Azuriaplysins A and B, Bromoditerpenes with an a-Methylene Carbonyl from the Sea Hare Aplysia kurodai

Structure Revision of Trichomide D by Total Synthesis

Total Synthesis of a PPAP, Nemorosonol, Using a Tandem Michael Addition-Intramolecular Aldol Reaction

A dynein-associated photoreceptor protein prevents ciliary acclimation to blue light.

Recent Progress in Structure-Activity Relationship Studies on Antitumor Macrolide Aplyronine A by Using Hybridization of Actin-depolymerizing Natural Product

A dynein-associated photoreceptor protein prevents ciliary acclimation to blue light

Synthetic Studies toward Aplysiasecosterol A: Concise Synthesis of the Tricyclic Core and Its Reactions for Introduction of the D Ring Fragment

Collaborators (8)

Keiko Hirose

Katsutoshi Mizuno

Ken-ichi Wakabayashi

Hitoshi Sawada

Takayuki Ohyoshi

Masahito Yoshida

Akira Noga

Takashi Ishikawa

Make your next move.

Hideo Kigoshi

Research Interests

Explore related searches

Contact this professor

About

Articles (21)

Concise total synthesis of (−)-berkelic acid <i>via</i> regioselective spiroacetal/pyran formation

Development of the “Molecular Glue” Using Hybridization of Natural Products,天 然 物 ハ イ ブ リ ッ ド 化 に よ る『 分 子 の り 』の 創 出

Skin- and airway-deliverable TRPA1 inhibitor

Structure revision of lagunamide C to odoamide by total synthesis and biological evaluation

Structure–Activity Relationship Studies on Scytophycin B, a Spiro-Epoxide-Containing Cytotoxic Macrolide

Total Synthesis of Aplysiasecosterols A and B, Two Marine 9,11-Secosteroids

Correction to “Isolation and Synthesis of Azuriaplysins A and B, Bromoditerpenes with an α-Methylene Carbonyl from the Sea Hare Aplysia kurodai”

Concise Total Synthesis and Biological Evaluation of Pargamicin A and its Diastereomer, Piperazic Acid‐containing Cyclopeptides

Concise total synthesis and structure revision of metacridamides A and B

Synthesis and Biological Evaluation of Siladenoserinol A Analogs Possessing a Diastereomeric 6,8-Dioxabicyclo[3.2.1]octane Skeleton

Toward the total synthesis of scytophycins: Synthesis of the C7–C21 fragments of scytophycins A, B, and C

Structure–activity relationship studies on an antitumor marine macrolide using aplyronine a–swinholide A hybrid

"Isolation and Synthesis of Azuriaplysins A and B, Bromoditerpenes with an a-Methylene Carbonyl from the Sea Hare Aplysia kurodai"(vol 85, pg 2082, 2022)

Bioinspired Total Synthesis and Structure-Activity Relationship Studies on Aplaminal

Isolation and Synthesis of Azuriaplysins A and B, Bromoditerpenes with an a-Methylene Carbonyl from the Sea Hare Aplysia kurodai

Structure Revision of Trichomide D by Total Synthesis

Total Synthesis of a PPAP, Nemorosonol, Using a Tandem Michael Addition-Intramolecular Aldol Reaction

A dynein-associated photoreceptor protein prevents ciliary acclimation to blue light.

Recent Progress in Structure-Activity Relationship Studies on Antitumor Macrolide Aplyronine A by Using Hybridization of Actin-depolymerizing Natural Product

A dynein-associated photoreceptor protein prevents ciliary acclimation to blue light

Synthetic Studies toward Aplysiasecosterol A: Concise Synthesis of the Tricyclic Core and Its Reactions for Introduction of the D Ring Fragment

Collaborators (8)

Keiko Hirose

Katsutoshi Mizuno

Ken-ichi Wakabayashi

Hitoshi Sawada

Takayuki Ohyoshi

Masahito Yoshida

Akira Noga

Takashi Ishikawa

Make your next move.

Development of the “Molecular Glue” Using Hybridization of Natural Products,天然物ハイブリッド化による『分子のり』の創出