Seijiro Hosokawa

Waseda University

Japan

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Articles (10)

The first total synthesis of marine isocyanide terpenes, halichonadins A–D has been achieved, featuring nitrile-to-isocyanide interconversion utilizing Hofmann rearrangement.

Year:

2024

Year:

2024

Year:

2024

Year:

2024

Year:

2022

Year:

2022

Year:

2021

Year:

2021

Year:

2020

Year:

2020

Collaborators (1)

Toshiya Masuda

Professor

Osaka University

JAPAN

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Seijiro Hosokawa

Research Interests

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Articles (10)

First synthesis of (±)-halichonadins A–D

Total syntheses of borolithochromes H1, H2, I1, and I2

Total Syntheses of Borolithochromes A, D and G

Synthesis of the C1–C13 Segment of Poecillastrin C

Total Synthesis of Alcyonolide

Bioinspired total synthesis of boneratamides A–C

Iodide-Mediated [3 + 2]-Cycloaddition Reaction with <i>N</i>-Tosylaziridines and α,β-Unsaturated Ketones

Synthesis of Polyacetate and Acetate-propionate Hybrid-type Polyketides Using Novel Remote Asymmetric Induction Reactions

Total synthesis of exigurin: The Ugi reaction in a hypothetical biosynthesis of natural products

Synthesis of Karrikinolide Using the Aldol-Type Acetal Addition Reaction

Collaborators (1)

Toshiya Masuda

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