Naoki Kanoh

Hoshi University — Japan

Chemistry · Physical Sciences

30h-index2.8kcitations166works1.32yr avg
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Research Topics

Synthetic Organic Chemistry Methods(43), Chemical synthesis and alkaloids(21), Marine Sponges and Natural Products(19), Microbial Natural Products and Biosynthesis(15), Advanced Biosensing Techniques and Applications(15)

Publications166 total

Synthesis of Cyclobuta[<i>cd</i>]pentalenes via an Intramolecular Double Michael Addition Reaction of 1,3-Cyclopentanedione Derivatives
Organic Letters·2025
Design and Synthesis of a 3-Arylenoyltetramic Acid Library Employing a Consecutive Three-Component Coupling
The Journal of Organic Chemistry·2025
PurA is the main target of aurodox, a type III secretion system inhibitor
Proceedings of the National Academy of Sciences·2024· 4 citedOpen Access
Correction to “Design, Synthesis, and Evaluation of Trivalent PROTACs Having a Functionalization Site with Controlled Orientation”
Bioconjugate Chemistry·2023
Asymmetric Total Synthesis of Cytotrienin A: Late‐Stage Installation of C11 Side Chain onto the Macrolactam Scaffold
Angewandte Chemie International Edition·2023· 4 citedOpen Access
Asymmetric Total Synthesis of Cytotrienin A: Late‐Stage Installation of C11 Side Chain onto the Macrolactam Scaffold
Angewandte Chemie·2023Open Access
<i>Cis</i> -Selective Double Spirocyclization via Dearomatization and Isomerization under Thermodynamic Control
The Journal of Organic Chemistry·2023· 7 cited
Naturally Occurring Polyene Macrolactams as Pluripotent Stem Molecules: Their Chemistry and Biology, and Efforts toward the Creation of Polyene Macrolactam-based Induced Pluripotent Small Molecules
Journal of Synthetic Organic Chemistry Japan·2022· 1 cited
Cis-selective double spirocyclization via dearomatization and isom-erization under thermodynamic control
2022· 1 citedOpen Access
Design, Synthesis, and Evaluation of Trivalent PROTACs Having a Functionalization Site with Controlled Orientation
Bioconjugate Chemistry·2021· 23 cited
Toward the Creation of Induced Pluripotent Small (iPS) Molecules: Establishment of a Modular Synthetic Strategy for the Heronamide C-type Polyene Macrolactams and Their Conformational and Reactivity Analysis
The Journal of Organic Chemistry·2021· 8 cited
Design, Synthesis, and Antifungal Activity of 16,17-Dihydroheronamide C and <i>ent</i> -Heronamide C
The Journal of Organic Chemistry·2021· 7 cited
A chalcone derivative suppresses TSLP induction in mice and human keratinocytes through binding to BET family proteins
Biochemical Pharmacology·2021· 7 cited
Design, Synthesis, and Evaluation of Trivalent PROTACs Having a Functionalization Site with Controlled Orientation
2021Open Access
Design, Synthesis, and Evaluation of Trivalent PROTACs Having a Functionalization Site with Controlled Orientation
2021Open Access
Design, Synthesis, and Evaluation of Trivalent PROTACs Having a Functionalization Site with Controlled Orientation
2021Open Access
Design, Synthesis, and Evaluation of Trivalent PROTACs Having a Functionalization Site with Controlled Orientation
2021Open Access
Toward the Creation of Induced Pluripotent Small (iPS) Molecules: Establishment of a Modular Synthetic Strategy to the Heronamide C-type Polyene Macrolactams and Their Conformational and Reactivity Analysis
2021Open Access
Design, Synthesis and Biological Activity of 16,17-Dihydroheronamide C and ent-Heronamide C
2021Open Access
Toward the Creation of Induced Pluripotent Small (iPS) Molecules: Establishment of a Modular Synthetic Strategy to the Heronamide C-type Polyene Macrolactams and Their Conformational and Reactivity Analysis
2021· 1 citedOpen Access
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Frequent Co-authors

Yoshiharu Iwabuchi(23), Hiroyuki Osada(12), Masatoshi Shibuya(10), Jun Ishihara(7), Akio Murai(7), Siro Simizu(6), Hiroyuki Yamakoshi(6), Masaya Nakata(6), Kaori Honda(5), Makoto Kawatani(4), Takeo Usui(4), Hiroyuki Shibata(4), Tsubasa Watanabe(4), Takamichi Imaizumi(4), Saori Kumashiro(3), Yasumitsu Kondoh(3), Satoru Hatakeyama(3), Hideo Tashiro(3), Makoto Muroi(3), Hisatsugu Ohori(3)