Great news, Planas' lab (@uri_planas) first project is finally on ChemRxiv!!! 🎉🎉🎉 Congrats to all the authors, and particularly to @fernando_selwin. So proud of being part of it!!
Zwitterionic Heavier Pnictinidenes in Redox Catalysis | ChemRxiv - https://t.co/V56REzDw1m
🚨Calling medicinal chemists🚨:
A Suzuki het-het coupling sometimes does not require complex ligands. An air stable Ni would do.
Amazing work from @rsaeb2 Rakan Saeb and Byeongdo Roh.
https://t.co/JpfG9dmLiz
Deciphering the mechanism of oxidative addition of aryl iodides into a red-light active bismuthinidene. Incredible team: Alexios Stamoulis,
@mato_mauro, Paolo Cleto-Bruzzese @MrIrieman, @GilSepulcre@CadraLab & Frank Neese. https://t.co/WpCGwvB73z
Transmetalating a challenging tetrel: introducing aryl-[Si] synthons into bismuth organometallic catalysis. Great work spearheaded by Teresa and Sophia. @angew_chem https://t.co/CJ7DEWXzK7
What happens when you mix carboxylic acids and pyridines? Acid-base reaction? You are only partially right. Check our latest article, isocyanates can greatly enhance the photochemical expansion of pyridines to 1,2-diazepines! @ILV_UMR8180 @XMoreau_ILV
https://t.co/JFP9HaLnNs
Check out this cool paper by @JenniferKuziola
Isolation of the first monomeric triarylbismuthine oxide, achieved by a novel approach as compared to lighter pnictine analogues
I'm excited to finally share my favorite project from my PhD journey at @CornellaLab (w/ @hyewon__moon , @MrIrieman , @Nils_Not_ , & @vabeland :
the monomeric triarylbismuthine oxide💎- the missing piece of the pnictine oxide series 🧩!
https://t.co/B17KflB42r
Expanding the horizons for bismuth as a redox catalyst. Now for cyclopropanation. @J_A_C_S https://t.co/FLZoHqFXI2 with @ShengyangN & @DavideSpinnato2
Happy to share this work from my PhD in @CornellaLab. Our “super naked“ nickel complex enables ligand exchange studies which are not accessible from classical precursors.
Thanks for the very nice collaboration @Nils_Not_ , it was really a pleasure :)
Here is our latest article on the chemistry of nickel. Super #naked nickel, sounds exciting doesn't it?! 😉 Thanks for another great stroy @CornellaLab and @rsaeb2! https://t.co/KA22Jqt9Dh
🚨📢 FULLY-FUNDED PhD POSITION! 📢🚨
Join my research team at the Institute of Organic Chemistry, 𝐔𝐧𝐢𝐯𝐞𝐫𝐬𝐢𝐭𝐲 𝐨𝐟 𝐕𝐢𝐞𝐧𝐧𝐚! Dive into cutting-edge synthetic organic chemistry and unravel complex reaction mechanisms. 🚀🔬
Start of an era! Thrilled to be back home to continue my academic career at @ciqususc ! Thanks a lot to
@MetBioCat for hosting me, and to my previous groups for all your support over the years! @CornellaLab@Echavarren_Lab
From flat common heteroaromatic rings to 3D dearomatized structures; our short review on modern dearomative enlargement reactions is now online in Synthesis @thiemechemistry
https://t.co/b2YREhFqZO
@XMoreau_ILV @ILV_UMR8180 @UVSQ_Research@uvsq
Thianthrene meets nickel catalysis!
We are happy to present our newest publication in @NatureCatalysis about C–heteroatom coupling of TT-salts with electron-rich aryls using nickel and light.
Great collaboration with @CornellaLab
https://t.co/6kIgTcy0N5
Previously on ChemRxiv, the final version of our photochemical protocol to convert pyridines into 1,2-diazepines in now out in @J_A_C_S! @ILV_UMR8180 @XMoreau_ILV
Our work is dedicated to the memory of Prof. Jacques Streith.
https://t.co/ioxuIhe7oP
We are looking for CSC PhD candidates for September 2024 start! Come join our lab in London🇬🇧⚗️ and explore sustainable organometallics♻️ with abundant metals!
⬇️
https://t.co/ganWP29HIB
Thrilled to see this work from my PhD in the Radosevich group published today in @J_A_C_S (w/ @theMarissaLava, Soohyun, @MylesDrance, @jeflip; in collaboration with BMS).
https://t.co/ONjJaPFrvU