Taichi Koike (@SiAdamas) header
Taichi Koike (@SiAdamas) profile picture

Dr.Sci., Assist. Prof., UTokyo | JST PRESTO | Former AvH Fellow | Unveiling the dance of reactive species with life and innovation | Posts in EN&JP |

orcid.org/0000-0002-6713-4375
Joined October 2021
Photo by Taichi Koike (@SiAdamas)Photo by Taichi Koike (@SiAdamas)Photo by Taichi Koike (@SiAdamas)Photo by Taichi Koike (@SiAdamas)Photo by Taichi Koike (@SiAdamas)Photo by Taichi Koike (@SiAdamas)Photo by Taichi Koike (@SiAdamas)Photo by Taichi Koike (@SiAdamas)Photo by Taichi Koike (@SiAdamas)Photo by Taichi Koike (@SiAdamas)
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/…
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余計ことを心配せず、学生と化学そのものに集中したい
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もっともっと頑張ろう。足りない。
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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
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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
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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/…
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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…
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🔬 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
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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
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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
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不安定化学種を研究するなら、実験環境に妥協しちゃ駄目だ。ほんとに駄目。 この1ヶ月、なかなか良いことがないけど、改めてその重要性を痛感した。 気持ちを切り替えていこう。
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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.
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東京大学で有機・高分子典型元素化学をやりたい方は、まず有機機能設計学研へレッツゴー
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小池助教がさきがけ(ゆらぎの理解と制御による材料革新)に採択されました!
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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!
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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🎉
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基礎有機化学討論会や
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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!
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