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Really proud to share our latest achievements in carbene-ring-opening chemistry!
A rapid & scalable route to azetidine-based methyleneketenimines unlocks multimodal reactivity.
Now online in @angew_chem .
Proud of this one. Huge shoutout to Keisuke!
onlinelibrary.wiley.com/doi/…
Taichi Koike retweeted
<プレスリリース> #創発的研究支援事業 における2026年度新規研究課題の決定について
jst.go.jp/pr/info/info1882/i…
2,519件の応募があり、243件の研究課題とその研究代表者を採択しました。
#JST #科学技術振興機構
Looking forward to the great science and conversations!
⏳ Time flies! IKCOC-16 is just around the corner—less than a month to go!
We can’t wait to welcome you all and enjoy inspiring lectures from our outstanding lineup of speakers!
ikcoc16.org/03.html
#IKCOC16 #OrganicChemistry
Taichi Koike retweeted
Our paper is now published in @J_A_C_S! 🎉
"π-Armor: Shape-Complementary Encapsulation of Aromatics"
A molecular prison for π-electron guests — no way out‼︎
Huge congratulations to Kano-san! 👏
@segawagroup @IMS1975
URL:
pubs.acs.org/jacsat/article-…
#supramolecular #hostguest
Taichi Koike retweeted
We are pleased to announce that our latest paper has been published in Organic Chemistry Frontiers!
In this work, we report the first direct catalytic synthesis of vinylic isonitriles through a new nucleophilic isocyanation strategy!
pubs.rsc.org/qo/article/doi/…
Taichi Koike retweeted
Our latest paper is out in @ChemicalScience! We revealed the potential of aminosulfoxonium leaving group for diastereodivergent transformation. Huge congrats to Taiga!
pubs.rsc.org/sc/article/doi/…
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 chemrxiv.org/doi/full/10.264…
Taichi Koike retweeted
🔬 PhD positions in electron microscopy × chemistry at NIMS, Japan (Apr 2027)
Atomic-resolution TEM of molecules
💴 ~200k JPY/month stipend
🎓 PhD from Kyushu Univ.
⏰ Deadline: Nov 12
Master’s required. DM me before applying!
🔁 RTs appreciated!
nims.go.jp/kyushu/en/junior/…
#PhD
Congrats, Avijit and the team! Great to see the next chapter of these molecules.
New paper in @J_A_C_S: NMR Evidence for magnetically induced ring currents in all-metal-aromatic [Bi₄]⁴⁺.
Congrats to all co-authors! Grateful to @AvHStiftung for supporting my postdoc at @UniHeidelberg. My first paper since joining @iitbbs!
doi.org/10.1021/jacs.6c14973
Congrats Fujimoto-san and the whole team! Excellent work!
Our new paper is out in @Nature ! 🎉
“Catalytic transfer of carbon atoms enables spirofusion of C–C σ-bonds”
Carbon-atom transfer turns planar molecules into 3D spiro frameworks through C–C σ-bond activation.
Congratulations to the whole team!
Read it here:rdcu.be/ysdKTXEbEbda
Hey glovebox experts! Is a dew point of −60 °C still too high for synthesizing highly reactive, low-coordinate species in a newly installed glovebox? We’re seeing a clear boundary. Some compounds still work, while others fail. Unfortunately, we need both! Solvents are great BTW.
JSTさきがけ ゆらぎ領域に採択していただきました。研究意欲が爆発しているので、精一杯頑張ります。何卒よろしくお願いいたします。#JSTさきがけ #JST_PRESTO @OFDLab_Tokyo @JST_Kisokenkyu jst.go.jp/kisoken/presto/app…
Can catalytic skeletal editing shift toward property control? In @ChemRxiv, we discuss this question across a range of organic materials and outline what catalysis could deliver next. Let’s push this chemistry!
It was great fun working on this with Sajan and Itami-san @Itamilab!
Can skeletal editing move from structural diversification to property control? Our Perspective on property-directed catalytic skeletal editing of functional organic materials is now on @ChemRxiv. Great work, Taichi @SiAdamas and Sajan!
chemrxiv.org/doi/full/10.264…
基礎有機化学会に、@OFDLab_Tokyo から澤くんと参加していました!
澤くんとご議論いただいた皆さま、ありがとうございました!
そして、澤くん、ポスター賞おめでとう🎉
It was a great pleasure hosting Asst. Prof. Javier Mateos @javiml_94 from the University of Vienna for an exciting lecture on selenium-based reaction development, followed by fruitful discussions with our faculty and students!
Always happy to reunite with friends!




















