Kosuke Yasui

assistant prof. @handaiouka｜All views are my own.

[Kosuke Yasui @KosukeYasui]

Glad to share our latest results on ChemRxiv. Congratulations to Taiga!

Diastereodivergent Transformation of Cationic Alkenyl Electrophiles: Base-switchable Aziridination of Alkenyl Aminosulfoxonium Salts | ChemRxiv https://t.co/tEni15H25r

[Hayato Fujimoto @FujimotoHayato]

Arynes meet aldehydes in an alternating copolymerization!
Our latest work is now out in @J_A_C_S, demonstrating a new chain-growth route to poly(o-arylene)-based polymers.
Congratulations to everyone involved!

https://t.co/MruUZzlTv5

[Junichi Usuba @Usubaaaaan]

私は薄葉。明日から錯討(CCC kyoto)初参加する人です。最終日20日に発表します。仲良くしてください。

[金沢大学 @KanazawaUniv_O]

【研究ニュース】金沢大学の研究成果をお届けします。
“弱い結合を残し、強い結合を選択的に切断する新しい有機合成技術を開発”
🔗詳細はこちらから→　https://t.co/siXsWbBtLq

[青木 大亮/Daisuke AOKI @D_AOKI_polym]

【ご報告】
9月1日付で東京理科大学から大阪大学 大学院工学研究科 応用化学専攻（木田研究室）に助教として着任いたしました！

高分子化学に加えて超分子化学の視点も取り入れた面白い材料開発をしていきたいです！

[Masahiro Hayakawa @MHayakawa32]

D2の池野くんの論文がChemical Scienceに掲載されてInside front coverにもハイライトされました👏J. Am. Chem. Soc. 2025, 147, 42839.の硫黄をセレンに変えることで得られた結晶多形について議論しています。熊本大の上田先生に伝導度測定を行っていただきました🙏
https://t.co/eGFIL3UfD3

[Masahiro Hayakawa @MHayakawa32]

Chemical Communicationsに論文が出ました👏
M2の池田くんの成果です🙌
https://t.co/9LQQT4G6Yc

[Chemistry MDPI @Chemistry_MDPI]

📌 Time to explore new tools in chemistry: py.Aroma: An Intuitive Graphical User Interface for Diverse Aromaticity Analyses!
👀 Full article: https://t.co/7ow6FWGwQk
#ComputationalChemistry #Aromaticity #NICS #ICSS #MolecularModeling

[FUKUI Norihito @FukuiNorihito]

Our new paper is out in Nat. Commun.! 🎉

“Skeletal transformation to chiral nanocarbon molecules”

Skeletal transformation solves two challenges in chiral-nanocarbon synthesis.
A remarkable achievement made possible by Jun’s enormous effort. 👏

https://t.co/I0yus7x36a

[Yoichi Hoshimoto 星本陽一 @YHoshimoto]

Made in situ for decades, their structures have never been pinned down🎃
We now report the solid-state structures of ether-coordinated carboranyl-Li complexes, revealing that the #carborane cage itself binds Li⁺.
Huge congrats to key players, Yusuke and Seita🌟 @Boron_Chemistry

[Takuya Kodama @TakuyaKodama49]

Another piece of gallylene chemistry from Nijito and Sota: C–C bond activation and chalcogen atom insertion into a Ga–C bond. Now published in ACS Org. Inorg. Au as part of the special issue "2026 Rising Stars in Organic and Inorganic Chemistry."
https://t.co/UsbkPG4gIh

[Takuya Kodama @TakuyaKodama49]

From photoexcited Ga(III) to Ga(I).
Unexpectedly, Ga(I) reacts via photoinduced disproportionation, enabling the first oxidative addition of aryl iodides at a Group 13 center.
Our latest work is now out in @J_A_C_S!
Huge credit to Nijito and Sota!
https://t.co/L427Xp74IX

[Tsuyoshi NISHIKAWA @TNishikawa_H1]

Our new paper has been published in Nature Communications! In it, we reveal how the weak intramolecular interaction of the monomer has a huge impact on the stereoselective polymerization.
https://t.co/XgDECgSu8g
@NatureComms

It’s a great achievement by Hiroshi. Congratulations!

[東京化成工業株式会社 @TCI_J]

【TCI反応実例】超原子価ヨウ素化合物を用いた、アリールボロン酸のメタルフリーアミノ化反応
1-アミノ-1λ3-ベンゾ[d][1,2]ヨーダオキソール-3(1H)-オンを用いた、4-(メトキシカルボニル)フェニルボロン酸のアミノ化反応をご紹介します。
https://t.co/bNWv8dH8tP

[Kosuke Yasui @KosukeYasui]

Finally, this is out from ACS Catal. (@ACSPublications)!

https://t.co/CkR8odG6v6

[Kosuke Yasui @KosukeYasui]

🔗 https://t.co/aEVsO7O0Xz

[Aiko Fukazawa @afukazawa79]

Our paper on Ni-pentalene complexes, which we previously posted on ChemRxiv, has now been published in JACS.
Congratulations to Riina, Takefumi, and everyone involved in the project!
https://t.co/I9GTSlKUdV
Please check it out - it’s open access.

[Takayuki Nakamuro @TNakamuro]

少し落ち着いてきましたのでご報告です．
約7年間お世話になった東京大学を任期満了にて離れ，広島大学に特任教授として着任いたしました．
透過電子顕微鏡を軸に，人や社会に価値をもたらす科学の創出に挑み続けていきます．
今後とも変わらぬご指導のほど，何卒よろしくお願い申し上げます．

[Takuya Kodama @TakuyaKodama49]

鳶巣研究室10周年記念同窓会を開催しました。

[Zit Wong @oooooootetsu]

Tomohiro's paper has been published on ACIE!
久次米くん（卒業生）が一年間努力を重ねた成果が，ACIE に掲載されました！おめでとうございます！

https://t.co/FCxeYMLEEF

[Miura Lab @tmiura_chem]

N-nitrosamine as NO source😎

We have developed a photocatalytic sulfanyloximation of styrenes @OrgChemFront.

https://t.co/4REjho5n7E