Electrochemical synthesis goes wireless @Nature! Congrats to Bartosz, @JonasRein_ and our friends in the McEuen lab. We’d like to also thank the Lennox Group for their highlight on SPECS:

RT @Nature: Electrochemical reactions for organic synthesis typically require intricate, specialized equipment, slowing progress in this fi….

RT @BetleyGroup: @SongLinLab I suSPECt this will be incredibly useful, nice work🫶.

RT @JonasRein_: Super excited to see our wireless electrosynthesis microchips in @Nature! SPECS make electrochemical reaction setup as easy….

Organic synthesis meets nanofabrication! Introducing SPECS: light-powered microchips that turn any well plate into a wireless high-throughput electrosynthesis reactor at the µL scale. Ideal for reaction discovery, optimization, and library synthesis!

All good things come in pairs😉 We’re excited to see these works out in @J_A_C_S today! Check them out:.

Farewell’s are also in order for our beloved post-docs Chenfei, Pierre-Louis and Bartosz🥹We’re sad to see you go, but can’t wait for what your new careers will have in store! Congrats!

We are thrilled to welcome five stellar 1st year students to the Lin Lab! Congrats to Bofei, Nayan, Evan, Joe and Xiaowei! Here’s to new friends and great science ahead🤩��️

Nothing brightens up a Monday morning like a successful PhD defense! Congratulations to the incredible Dr. @Zhipengluu🤩 Wishing you the best of luck as you begin your career @TakedaPharma 🎉

RT @JonasRein_: Super happy to share these two works by our aminoxyl team: Oxoammonium catalyzed hydride abstraction for selective C–H oxid….

RT @ThePatilGroup: Call for Papers for Joint Special Issues in Tetrahedron Letters and Tetrahedron in honor of Prof. Eric Jacobsen and Prof….

@YukunCheng1 developed the catalytic oxidation of weakly hydridic ethers with either mCPBA or e-chem⚡️. Through a novel relaxometry based NMR experiment for in-situ radical quantification, we unraveled the delicate equilibria among multiple resting states!

@JonasRein_ and Bartosz developed a catalytic, mild, and selective oxidation of N-substituted amines through HTE and stereoelectronic tuning of aminoxyl radicals. With the help of @BoehringerUS, we then scaled up in batch and flow! (2/3).

No hydridic C–H bond is safe! Back to back in @ChemRxiv today, we report oxoammonium catalyzed oxidation of N-substituted amines and ethers! Featuring high TON, 100 g scale-up, a novel NMR experiment for radical quantification, & QSPR! (1/3)

RT @J_A_C_S: α,β-Desaturation & Formal β-C(sp3)–H Fluorination of N-Substituted Amines: Late-Stage Functionalization Enabled by Electrochem….

ShoNo? More like ShoYes! Now in @J_A_C_S, an electrochemical protocol for α,β-desaturation of N-substituted amines, providing convenient access to β-C–H fluorinated products! A phenomenal group effort by Luiz, Justin, Kaining & our friends at @Genentech⚡️

Past and present Lin Lab members Lingxiang, Samson, Cindy and Bartosz are charged up for this year’s Stereochem GRC!⚡️

Congrats to Dr. @JonasRein_ on a phenomenal PhD defense! A brilliant mind, asymmetric catalysis wizard, and exceptional mentor, your guidance has been invaluable to us all⚡️🧑‍💻Here's to your well-deserved success and many future achievements to come!

Rising 2nd year Sukwoo also gave an awesome department seminar on his contributions to this work! We are SO proud🤩 Watch out for more to come from this superstar🎉

Out now in @J_A_C_S! @ju_minsoo, Sukwoo and Halle describe a convenient approach for accessing frustrated radical pairs from tertiary alcohols. We had so much fun scaling up & elaborating our FRP chemistry towards complex molecule synthesis! Check it out: