Access SEAr-type products in typically disfavored positions! Contratulatons to Rita, @jyotirmoydey.bsky.social and Elisa showin in Org. Lett. how nondirected C-H activation and oxidative cleavage can be used to obtain challenging regioisomers in formylation and carboxylation doi.org/10.1021/acs....

A simple, scalable method by Jurk & van Gemmeren @vangemmerenlab.bsky.social to convert secondary sulfonamides into sulfonyl fluorides using affordable #DAST ⚗️, yielding excellent results! These sulfonyl fluorides readily couple with amines to create diverse libraries. #SuFEx 👉 buff.ly/hjkyEap

The final version of our @vangemmerenlab.bsky.social 'Molecular Stitching' approach, enabling one-step access to a diverse library of γ-alkylidene lactones, is now out in @chemicalscience.rsc.org #MyFirstChemSci Link to the full article: doi.org/10.1039/D5SC...

Congratulations to aol three @uni-kiel.de candidates who were selected to participate in the Lindau Nobel Laureate meeting. In particular of course our very own @sourjyamal.bsky.social. A well deserved recognition of his excellent doctoral studies. #proudPI #chemsky www.uni-kiel.de/de/detailans...

Great job Edis and @sourjyamal.bsky.social! Their work on the synthesis of γ-Alkylidene Lactones has just been accepted for publication in the @rsc.org journal @chemicalscience.rsc.org doi.org/10.1039/D5SC...

Just saw on the OL homepage that the article currently leads the journals most read list, thanks for all the interest in our work! pubs.acs.org/action/showM...

Check out our newest C(sp³)–O bond formation strategy: doi.org/10.1021/acs....

Congratulations to Edis and @sourjyamal.bsky.social, who have completed their studies on a new and efficient approach towards gamma-alkylidene lactones directly from carboxylic acids and lactones now posted on @chemrxiv.bsky.social chemrxiv.org/engage/chemr... #chemsky #chemistry

Check out my latest preprint from @vangemmerenlab.bsky.social , where we disclosed a one-step approach to access γ-alkylidene lactones by stitching together aliphatic acids and styrenes, enabled by N-Acyl Sulfonamide ligand. doi.org/10.26434/che...

Thanks for all the interest in the study. It is now amongst the currently most read in ACS Catalysis

Smashing distal C–H bonds of the unprecedented β-non-quaternary acids has been a formidable task over the years; several years of our involvement in 'Ligand Design' finally broke the deadlock! Thanks to @vangemmerenlab.bsky.social for guiding us to achieve this feat !

We have developed a direct gamma-lactonization of carboxylic acids. The scope includes beta-non-quaternary subatrates that were until now out of reach for carboxylic acid gamma-C-H activation. Congratulations to Tianxiao and Sourjya. Have a look at the study now posted on ChemRXiv t.co/Wu0XtwsEQR

Our work on the direct fluorination of carboxylic acids has just appeared in @NatureSynthesis! (www.nature.com/articles/s44...). This terrific study bySourjya Mal, Friedrich Jurk, and Kerstin Hiesinger is highlighted in a press release by our University: www.uni-kiel.de/en/details/n...