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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:
Song Lin Lab
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Song Lin Lab
@SongLinLab
Electrifying organic chemistry since 2016 | Cornell University | For group updates, find us on LinkedIn!
- Big news today – we just heard that our very own @songlin_chem has been promoted to Associate Professor with tenure @CornellChem!! Congratulations Song!!! Here we are, then and now:
- Our latest work on electrochemical C(sp3)-C(sp3) cross-electrophile coupling is now in print! This came out of a fun collaboration with @The_See_Group and our friends at @Merck. Read all about it in @Nature: nature.com/articles/s4158…
- We are thrilled to share our latest paper in collaboration with Yu lab: “Electrochemical reactor dictates site selectivity in N-heteroarene carboxylations”. Check out the pre-proof version in @nature: nature.com/articles/s4158… 1/3
- Check out our latest work in @Nature - Through leveraging frustrated radical pairs we accessed adaptive C-H activation using a variety of disilazide donors and N-oxoammonium acceptors, producing an array of alkoxyamines. nature.com/articles/s4158…
- We are thrilled to share our recent work in electrochemical C(sp3)-C(sp3) cross-electrophile coupling! Check out our latest @ChemRxiv where we showcase the selectivity afforded by electrosynthesis! @echemkim @dan_lehnherr @NSF_CSOE chemrxiv.org/engage/chemrxi…
- Congratulations to our fearless leader for being named Tisch University Professor, one of Cornell University’s highest faculty honors! We’re proud to call you our boss 🙌 @songlin_chemWe are pleased to announce that Song Lin has been appointed Tisch University Professor. This promotion recognizes Song’s outstanding contributions to the field of organic electrochemistry and to the Cornell community. Congratulations, Song!
- Introducing HTe-Chem: Today we bring you an exciting new venture into electrochemistry--the development of a new #HTE system for the rapid optimization of electrochemical reactions! Congrats to Jonas, James, and to our collaborators @Merck! @ChemRxiv chemrxiv.org/articles/prepr…
- We’re excited to share our latest work in @J_A_C_S⚡️ Leveraging the redox activity of in-situ generated trialkyl borates, we developed an electrochemical protocol to convert alcohols, aldehydes, & ketones into boronic esters. Congrats @WeiyangGuan & Yejin!
- Online today in @J_A_C_S- An electroreductive approach for cross-electrophile dialkylation of alkenes! Congratulations to @lingxiang_lu, Yi Wang, and our wonderful collaborators in the @echemkim lab⚡️
- ⚡️We're excited to share our latest work on electron-initiated hydrofunctionalization of alkenes in @J_A_C_S! This work is part of a great collaboration with Abruña lab⚡️ @CornellChem @NSF_CSOE ⚡️
- We're excited to bring you the latest chapter in our electroreductive chemistry saga! In this work, we use electrochemically-generated silyl radicals to enable a diverse suite of valuable silylation reactions. Appearing now on @ChemRxiv: doi.org/10.26434/chemr…
- 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)
- Check out our latest publication in @NatureChemistry, where we team up copper + cobalt to facilitate ⚡ enantioselective alkene hydrocyanation! Congrats to Lu, Kai, and Will! nature.com/articles/s4155…
