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Happy to share this work from my postdoc in Cornellab (w/ Feng, Oriol Planas, Markus L., @Nils_Not, Kalishankar, Alex)! We demonstrate mechanistic studies on Bi-catalyzed transfer hydrogenation via Bi(I)/Bi(III) redox cycling. onlinelibrary.wiley.com/doi/10.1002/an…

Thrilled to see this work from my PhD in the Radosevich group published today in J. Am. Chem. Soc. (w/ Marissa Lavagnino, Soohyun, Myles Drance, Jeff Lipshultz; in collaboration with BMS). pubs.acs.org/doi/10.1021/ja…

We are looking for CSC PhD candidates for September 2024 start! Come join our lab in London🇬🇧⚗️ and explore sustainable organometallics♻️ with abundant metals! ⬇️ planaslab.com

Previously on ChemRxiv, the final version of our photochemical protocol to convert pyridines into 1,2-diazepines in now out in J. Am. Chem. Soc.! @ILV_UMR8180 @XMoreau_ILV Our work is dedicated to the memory of Prof. Jacques Streith. pubs.acs.org/doi/10.1021/ja…

Congrats! So proud of you 🎉

Happy to see some of my PhD research in Cornellab online. Thanks and congrats to everyone involved! chemrxiv.org/engage/chemrxi…

Amination of heterocycles with naked nickel, now in ChemRxiv by Rakan Saeb and Bryan B. chemrxiv.org/engage/chemrxi…

[W]+ with Davide Spinnato, Nils.Not, Markus L., M. van Gastel, L. Wagner and F. Neese chemrxiv.org/engage/chemrxi…

Thianthrene meets nickel catalysis! We are happy to present our newest publication in Nature Catalysis about C–heteroatom coupling of TT-salts with electron-rich aryls using nickel and light. Great collaboration with Cornellab doi.org/10.1038/s41929…

From flat common heteroaromatic rings to 3D dearomatized structures; our short review on modern dearomative enlargement reactions is now online in Synthesis Chemistry at Thieme thieme-connect.com/products/ejour… @XMoreau_ILV @ILV_UMR8180 UVSQ Research UVSQ

Start of an era! Thrilled to be back home to continue my academic career at CiQUS ! Thanks a lot to Mascareñas group for hosting me, and to my previous groups for all your support over the years! Cornellab Echavarren Lab

🚨📢 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. 🚀🔬

Happy to share this work from my PhD in Cornellab. 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 :)

Expanding the horizons for bismuth as a redox catalyst. Now for cyclopropanation. J. Am. Chem. Soc. pubs.acs.org/doi/epdf/10.10… with Shengyang Ni & Davide Spinnato

Check out this cool paper by Jennifer Kuziola Isolation of the first monomeric triarylbismuthine oxide, achieved by a novel approach as compared to lighter pnictine analogues

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 onlinelibrary.wiley.com/doi/10.1002/ad…

Transmetalating a challenging tetrel: introducing aryl-[Si] synthons into bismuth organometallic catalysis. Great work spearheaded by Teresa and Sophia. Angewandte Chemie onlinelibrary.wiley.com/doi/10.1002/an…

Deciphering the mechanism of oxidative addition of aryl iodides into a red-light active bismuthinidene. Incredible team: Alexios Stamoulis, Mauro Mato, Paolo Cleto-Bruzzese Markus L., Marcos Gil Sepulcre Alejandro Cadranel & Frank Neese. pubs.acs.org/doi/10.1021/ja…

🚨Calling medicinal chemists🚨: A Suzuki het-het coupling sometimes does not require complex ligands. An air stable Ni would do. Amazing work from Rakan Saeb Rakan Saeb and Byeongdo Roh. onlinelibrary.wiley.com/doi/10.1002/an…

Great news, Planas' lab (Oriol Planas) first project is finally on ChemRxiv!!! 🎉🎉🎉 Congrats to all the authors, and particularly to Selwin Fernando. So proud of being part of it!! Zwitterionic Heavier Pnictinidenes in Redox Catalysis | ChemRxiv - go.shr.lc/4bfooqH