We have a 3.5 year PhD studentship available in the group (@UofChem) for an October 2025 start. If you are interested in organic synthesis and developing new imaging agents, see: https://t.co/VSQ5kKGYyF
RTs appreciated.
We have a PhD position available in organic synthesis - come and join the group that made @jeff940317 and @GeordieChemist the scientists they are today!
https://t.co/wzgzoxnaa4
Excited to share our latest work on androgen receptor NTD antagonists out now in ACS Med Chem Lett @ACSBioMed@StrathChem@aberdeenuni
https://t.co/NcTLDxEFMl
@LeResearchGroup @dcadwallader94 @felixfelicisll@JOC_OL Really nice work! A non-trivial transformation and you make it look easy! Will definitely give this one a go at some point.
Happy to share our latest paper on the fluoride-catalyzed synthesis of alkynamides from carbamoyl fluorides!
@dcadwallader94, @felixfelicisll, and Tristan demonstrate how a common reagent can be a highly active catalyst, now live in Org Lett (@JOC_OL) https://t.co/NhOL8uKjse
A 5-year MRC funded postdoctoral position to work on the development of new PET imaging agents and radiochemical methods is available in the group (@UofGChem). See the following to apply: https://t.co/79UXElLCn1
RTs appreciated. 👍
Pleased that our work was recently published in @JOC_OL
Direct trifluoromethylthiolation of aromatic amino acid residues leads to an unprecedented increase in peptide hydrophobicity
For more details, check out the ASAP article:
https://t.co/U6jQYrH1NL
@IskraJernej (UL) @BioCIS
The first paper from the group is out today in @J_A_C_S !!! 🥳
Check out our approach for the synthesis of the eburnane alkaloids. Many thanks to Krishna, @LarisaPop737, @ZurwaCheema, Harish, @LucaSan01410777... keep up the great work! @UTDallasChemBio
https://t.co/PP0LxDiL2A
New paper from the group just published @JOC_OL on pyrimidine-based amino acids that have pH and polarity sensitive fluorescence. Congratulations to Sineenard and Alex! (@UofGChem)
https://t.co/Cx6TMQxPu4
Opening new doors: Rapid access to arynes via formal dehydroboration of arylboron compounds. Learn more in the #OrgLett article from @dstuartgroup https://t.co/XMOqNbZ5WQ