Our work on Decarboxylative Metal-Halogen Exchange has been higlighted in @OPRD_ACS 💡 Thank you to the team behind the OPRD highlight 🙇
https://t.co/SGNIh0Z7tY
Our work with Sally Bloodworth at the Physical Sciences Data Infrastructure (PSDI) has been published in Synlett @thiemechemistry
👉https://t.co/RveCIBcDWC
We hope this contributes positively to the ongoing discussion on reproducibility in organic synthesis.
Thanks to Paul Richardson (Pfizer) for highlighting our recent work in Synfacts @thiemechemistry 💡
Synfacts link: https://t.co/kk2fEFYl4e
The work was led by Danny Ryder and involved a great collaboration with @KenYamazaki5.
Original paper: https://t.co/zEb9oCLM01
Thanks to @CambeiroChem and @KLchemistry for hosting me @UniofGreenwich. A beautiful campus steeped in maritime history ⚓️ (...and a distillery nearby 🍸). Great discussions with fantastic staff and super bright students! Looking forward to #Syntech2026 in July.
Well done to the team, especially Grace Beaver who set off this pursuit by doing a fantastic job in their 3rd year undergraduate literature review project.
Our review on CO2 Transfer and Carbon Isotope Exchange is out in Organic Chemistry Frontiers. @RoySocChem
Thank you to the editors for the highlight in their Emerging Investigator Series 🙇
https://t.co/IURvLsFINd
@UoSChem_ChemEng , @AstraZeneca
Our latest work on Dual-Function Reagents is now out in @ChemCommun. Thank you to the editors for the highlight in their Emerging Investigator Collection 🙇
Fantastic work led by Katherine Marris 🥼 Great team effort @UoSChem_ChemEng, @AstraZeneca 🎉
https://t.co/si9ZxAVbyV
Our work on Decarboxylative Metal-Halogen Exchange is out now in JACS Au @ACSPublications 🙌
Brilliant work by Danny Ryder 🥼 and a great collaboration with @KenYamazaki5 💻
https://t.co/k8XWdv73Gh
Check out the robustness screen in the SI too - it nicely illustrates the tolerance that this metal-halogen exchange-type process has towards ketones, nitriles, alkyl halides and more! 💪
A Para-Selective Kolbe-Schmitt Reaction out now in @angew_chem 🚨
https://t.co/JUzDXN3Y64
No need for high-pressure CO2, excessive temperatures or stringently dry conditions. Our carboxylating reagent unlocks a simple Kolbe-Schmitt-type reaction with unique para-selectivity.
ジベンゾチオフェンジオキシドの光還元的分子変換に関するPerry Group @PerryChemとの共同研究が、Chem. Sci.誌@ChemicalScienceに公開されました!
Check out our latest collaboration paper in https://t.co/LxQIRx1dzy
Open to UK students and those eligible for a Horizon Europe fee waiver list:
https://t.co/hoob35zQLs
Other international applicants will have to be competitive to apply for a Presidential bursary:
https://t.co/DdgVLrXtLN
We have a fully-funded PhD position available in our group. For those interested in organic synthesis and developing their lab skills.
Feel free to get in touch for informal enquiries.
https://t.co/ItGCmQKB6V