EurJOC誌に掲載決定!

Efficient Visible-Light-Induced π-Extension of Perylene Tetraesters: An Investigation on Regioselectivity
Keisuke Fujimoto, Shingo Miyano, Kenshin Norizuki, Toshiyasu Inuzuka, Tetsuya Sengoku, and Masaki Takahashi
European Journal of Organic Chemistry, 2024, 27, e202400734. (DOI: 10.1002/ejoc.202400734)

This study reports a visible-light-induced π-extension of perylene tetraesters using blue LED irradiation. The synthesis revealed how substituent effects on aromatic groups influence regioselectivity. Theoretical analysis highlighted bond alteration in aromatic rings as a key factor.

European JOC誌に掲載決定!

Synthesis of Highly Emissive Fluorophores Based on Multiply Stacked Anthracene Arrangement
Keisuke Santo, Kentaro Uchida, Keisuke Fujimoto, Toshiyasu Inuzuka, Kazutaka Hirakawa, Tetsuya Sengoku, and Masaki Takahashi
European Journal of Organic Chemistry2023, e202201479. (DOI: 10.1002/ejoc.202201479)

Journal Information: Impact factor 2.8 (Q2, JCR 2023)

浅羽君、Luaさんの論文がJOC誌に掲載決定!

Controllable monobromination of perylene ring system: synthesis of bay-functionalized perylene dyes
Masaki Takahashi, Kyohei Asaba, Trinh Thi Lua, Toshiyasu Inuzuka, Naohiro Uemura, Masami Sakamoto, Tetsuya Sengoku and Hidemi Yoda
The Journal of Organic Chemistry, 2018, 83, 624-631. (DOI: 10.1021/acs.joc.7b02540)

Practical synthesis of bay-monofunctionalized perylene dyes has been developed based on controllable NBS bromination of tetrabenzyl perylene-3,4,9,10-tetracarboxylate. The ability to perform the convenient and high-yielding synthesis highlights the potential utility of our multifunctional approach to access diverse range of new perylene systems.

Journal Information: Impact factor 4.849 (Q1, JCR 2016)

Publication (~2016)

*2008年以降の論文のタイトルは掲載論文webサイトにリンクしています。

  • Invited review for a special issue on “New aspects in natural product synthesis: methodology and strategy
    Evolution of the Total Syntheses of Batzellasides, the First Marine Piperidine Iminosugar.
    Tetsuya Sengoku, Jolanta Wierzejska, Masaki Takahashi and Hidemi Yoda, Natural Product Communications 2013, 8, 1011-1019.

  • Invited article for a special issue on “New aspects in natural product synthesis: methodology and strategy
    Synthetic approach toward α-aminomethyl-γ-butyrolactones from β-lactam synthons elaborated by SmI2-mediated reductive coupling reactions.
    Masaki Takahashi, Takahiro Sudo, Yusuke Murata, Tetsuya Sengoku and Hidemi Yoda, Natural Product Communications 2013, 8, 889-896.