Organic chemist, husband, father. Work: University of Gothenburg. Like: organic synthesis, OTHO gels, reggae
Joined May 2013
- Tweets719
- Following813
- Followers563
- Likes976
Excited to hear about the latest developments in organic chemistry in Sweden! Don’t miss out—join us at tomorrow's event!🧪🧪
👉 eventbrite.ie/e/highlighting…
#EuChemS
Henrik Sundén retweeted
We are delighted to share our study of Diels–Alder cycloadditions of oxacyclic allenes and pyrones. Congrats to Laura, Milauni, Lisa, and Sarah! #WomeninSTEM @uclachem Read it here: doi.org/10.1021/acs.orglett.…
Congratulations to a fantastic work both of you. Happy that you choose @sundenlab to do your diploma work.🎉
Congratulations to Michelle and Jonatan for earning your Bachelor's degree! Your exceptional thesis and impressive presentation made me incredibly proud. Excited for your bright future. @OMC_GU @sundenlab #BoronChemistry
Henrik Sundén retweeted
#MSCA fellowships! Join our thriving group @docklahn, klahnlab.de Develop covalent inhibitors & extra cellular targeted drug conjugates! DM for info!
This Post is from an account that no longer exists. Learn more
#MSCA fellowships! Join our thriving group @SundenLab (2x successful applications!). Develop organic synthesis methods & functional gels. DM for info!
This Post is from an account that no longer exists. Learn more
Henrik Sundén retweeted
Finally, our review on aryl O-carbamates as DMGs (published with the late world-renowned chemist, prof Vic Snieckus) is online!
Thanks for all the hard work & support, @KosmrljGroup @ACSChemRev @unilj @Rajshahivarcity @queensu @QueensChem @EutopiaUni.
doi.org/10.1021/acs.chemrev.…
ALT The aryl O-carbamate (ArOAm) group is effective in Directed ortho Metalation (DoM) and the Anionic ortho-Fries (AoF) rearrangement, among a range of highly useful transformations. In addition, the ArOAm group can be converted into a diverse range of functionalities e.g., OH, via reductive cleavage, and coupled with various groups through a spectrum of cross-coupling (CC) strategies. This review covers the latest developments in the chemistry of the ArOAm group since 1990 (the last time it was reviewed).
Henrik Sundén retweeted
I just wanted to promote the recently established Victor Snieckus Foundation victorsnieckusfoundation.ca, set up to support future postdoc research fellows and empower the next geenration of organic chemists!
Henrik Sundén retweeted
Time is ticking! ⏰ Don't miss out on #ECC9 in Dublin! Standard Registration Fee closes in just 1 week. Register now and join us for an unforgettable experience! euchems2024.org/registration…
Henrik Sundén retweeted
Emil Sandelin from @wallentin_carl group defending his PhD thesis „Breaking the cage – Implementing photocages to address spatiotemporal challenges in chemical biology“after Arwen R. Pearson from @unihh introduced the audience to the field! @goteborgsuni @Naturvetenskap
Henrik Sundén retweeted
Check out our latest work in @JOC_OL! Making amides through decarboxylative cross-coupling between carboxylic acids and isocyanides. Great collaboration with the Liu and Wang groups!
doi.org/10.1021/acs.orglett.…
Henrik Sundén retweeted
Check out our research into thermo-responsive PAGs as draw agents for forward osmosis (50 days' free access to the article, from today!); a neat collaboration between @unilj and Uni of Maribor (Slovenia). authors.elsevier.com/c/1izU9…
@KosmrljGroup @EutopiaUni
@DesalinationJ
🎉 Exciting news! 🎉 Sara and Simon's paper on redox-active NHCs is now among the most read articles in the past 30 days. #carbenes @OMC_GU 📄🔬Check it out here: Redox Active N-Heterocyclic Carbenes in Oxidative NHC Catalysis | Organic Letters pubs.acs.org/doi/abs/10.1021…
Henrik Sundén retweeted
Sara Bacaicoa presenting the latest publication of @sundenlab on our floor meeting! Congrats to this fantastic work! pubs.acs.org/doi/full/10.102…
@sundenlab @goteborgsuni @Naturvetenskap
Henrik Sundén retweeted
Next chapter in our hypervalent adventure! how would you access polyhalogenated biaryls in a perfectly selective way? Great collaboration with @Merck @chair_itn! congratulations to @danielcarter_96 Maxime et @PascalHauk pubs.rsc.org/en/content/arti…
Henrik Sundén retweeted
What is better? In situ generated complex Or air-stable, fully character isolated catalysts ? To answer this please check our first C-H borylation paper! Great collaboration with @Syngenta @chair_itn ! Congratulations to Janis and Tomas! onlinelibrary.wiley.com/doi/…
Henrik Sundén retweeted
If @GawelPrzemyslaw could be granted a superpower, what would it be? @IOC_PAS Find out on his #IntroducingAngewandte page xitter.cf/16467437/status/176866… onlinelibrary.wiley.com/doi/…
Singlet Fission in a New Series of Systematically Designed Through-space Coupled Tetracene Oligomers (Przemyslaw Gawel and co-workers) @GawelPrzemyslaw, @IOC_PAS, @MajdeckiMaciek #openaccess onlinelibrary.wiley.com/doi/…
Henrik Sundén retweeted
👉 We were thrilled to welcome Prof. Dr. Henrik Sundén (@sundenlab) from the University of Gothenburg 🇸🇪 at UL FCCT. 🇸🇮 Thank you for an engaging presentation 📢 on synthesizing oxotriphenylhexanoates (OTHOs) and their role in forming supramolecular gels! 🧫
Henrik Sundén retweeted
We explored potential ground & excited state (anti)aromaticity of 3,4-dimethylenecyclobutene and designed macrocycles with tentatively interesting features, some with low-energy nonet states (@preethanuj106 @RoldaoJuan @dcasanova_dipc)
Now in @ChemEurJ
chemistry-europe.onlinelibra…
Henrik Sundén retweeted
Exciting news from @sundenlab! 🧪 Discover how they're merging oxidants and carbenes in one hybrid catalyst for cutting-edge organocatalysis. See the work in #OrgLett pubs.acs.org/doi/10.1021/acs…. Many thanks to @SaraBacaicoa and Simon for their dedication and hard work! #Carbenes
Henrik Sundén retweeted
Oxygen is enough!! And it works great for the synthesis of 12 natural products!! Many congrats to Kiki Gennaiou and Antonis Kelesidis!
Climbing the Oxidase Phase Ladder by Using Dioxygen as the Sole Oxidant: The Case Study of Costunolide | Organic Letters pubs.acs.org/doi/10.1021/acs…
