It's out! Find out how α-Keto Acids can help you in acylation reactions. This dorment reagent can participate in an incridible number of transformations @PenteadoFilipe @EderLenardao #acylating #Review #Organicchemistrty #justlikesleepingbeuty #synthesis pubs.acs.org/doi/10.1021/ac…

Finishing up Halloween with an awesome decoration from our NMR department @ufrgsoficial

Meet ReShiki v0.9: Chemical drawing, reinvented.

New in v0.9:
• More publisher drawing styles
• Custom color themes
• Light/dark mode support
• Improved aromatic ring fusion

Try it → reshiki.com
Star the repo ⭐ github.com/Ameyanagi/ReSh…

This one is very special to me: Check out out latest work on extended azulenes! Out now in ⁦@ChemistryEur⁩ …mistry-europe.onlinelibrary.wiley.com/doi/10.1002/ce…

C&EN (@cenmag) agrees that skeletal editing is revolutionizing chemistry! In a recent feature, Prof Mark Levin discusses "cutting and pasting" atoms, a new method that enables chemists to fine-tune drugs with unprecedented control. Read more here: cendigitalmagazine.acs.org/2025/07/10/ske…

I'm very happy to see the second work from my PhD now online at @JACS_Au . Thanks to all the authors, especially Professors Diogo Lüdtke and Fabiano Rodembusch (@photochem_UFRGS) for all these years of collaboration. | JACS Au pubs.acs.org/doi/10.1021/ja…

What we have being working for this last six months is finally out, this was part of my first post doc work with prof @juliopastre. Great working with @RodrigoCosta18 for this project
aces.onlinelibrary.wiley.com/doi/10.1002/as…

One of the projects from my PhD was published! Had a wonderful time making this project with @MCDietl at the Hashmi group @UniHeidelberg

…mistry-europe.onlinelibrary.wiley.com/doi/10.1002/ch…

This brings good memories from when I was with the maulide group! Nice to see it published

PyrAtes: Modular Organic Salts with Large Stokes Shifts for Fluo-rescence Microscopy (Nuno Maulide and co-workers) @MaulideLab #openaccess onlinelibrary.wiley.com/doi/10.1002/an…

#OnTheCover Bioinspired Selenium-Nitrogen Exchange (SeNEx) #ClickChemistry Suitable for Nanomole-Scale Medicinal Chemistry and Bioconjugation (Hongtao Xu and co-workers) onlinelibrary.wiley.com/doi/10.1002/an… @ShanghaiTechUni @HelloZJUT onlinelibrary.wiley.com/doi/10.1002/an…

It’s out! Check our @Nature publication about charge relocation!

nature.com/articles/s4158…

Congratulations to the team!
#Bogdan @GiuliaIannelli @el_salato #oxacarbeniumgang

great opportunity and great people behind the program, worth applying

A big day for "carbyne"- the elusive sp carbon allotrope. It literally took decades of synthetic expertise from chemists around the globe to make functional equivalent of that enthralling "all carbon" gem! (1/4)
pubs.acs.org/doi/epdf/10.10…

Light-Driven Enantioselective Carbene-Catalyzed Radical-Radical Coupling (Karl A. Scheidt and co-workers) @ScheidtGroup @PHYCResearchLab onlinelibrary.wiley.com/doi/10.1002/an…

Pyrylium lovers, check this out! I'm thrilled to share our 2 back-to-back procedures out today in @OrgSynth from @CornellaLab. We report the gram-scale synthesis of Pyry.BF4 and its late-stage use in the preparation of arylsufonyl fluorides. Go use it! orgsyn.org

I am very happy to see our most recent article published in @Orgmet_ACS ! Check it out, it is about the synthesis of protic NHC metal complexes! Stay tuned, there is more to come😌 pubs.acs.org/doi/10.1021/ac…

Copper catalyzed Ullmann couplings are one of the oldest ways to forge new bonds. Our new mechanistic study in @ScienceMagazine shows these reactions occur by a novel mechanism: leading to higher TONs, more stable catalysts, and air tolerant conditions! doi.org/10.1126/scienc…

Delighted to have the chance to tell the full story of our recent research using organogels to stabilise organolithium reagents, allowing them to be safely handled in air - from concept to implementation, patent to paper.
Read all about it in Synform: thieme.de/statics/dokume…

Wanna try out some S-olefination reactions inspired by our recent @J_A_C_S publication?
We’re shipping 1 g samples of thiouronium *free of charge*, for you to try the reaction in your lab!
Go to maulide.univie.ac.at/news/news-deta… and claim your sample now @univienna #chemtwitter #ylide