the Strand group
@thestrandgroup.bsky.social
Social media outlet for the Strand group, Lund University – research driven by synthesis and a bit of curiosity.
Our work on the synthesis of (+)-chetomin, along with its natural and unnatural congeners, is now available at ChemRxiv: doi.org/10.26434/che... We look forward to the many opportunities for exciting biology and synthesis that will arise from this study. Well done to all involved!
It's been a long time coming. Pleased to share our synthesis of siphonazole B lead by Filip Paulsen. Check out the domino rearrangement sequence - its neat: chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/...
Synthesis of Siphonazole B Through Domino Cycloisomerization‐Oxazolonium Ion Rearrangements
The study by Strand and co-workers describes a concise synthesis of siphonazole B. Both oxazole units are formed from a simple propargylamine using a novel domino cycloisomerization-rearrangement app...
chemistry-europe.onlinelibrary.wiley.com
Out of 12 high quality submissions from Sweden the jury of the Nordic Retrosynthesis Challenge has selected 6 teams, which are now proceeding into the second round. Congratulations to At Least No Nitrogen, Eduardoncita’s Lab, KK4, Masters in Cleavage, Carboga and Tralling for Terpenes
The molecule is live, and the hype is real. Good luck to everyone who is participating #NordicRetrosynthesisChallenge
