Check out our latest work. Now published in Angewandte Chemie on " Sulfonium Cation in the Service of π-Acid Catalysis" onlinelibrary.wiley.com/doi/epdf/10.10…

Very pleased to embark on the PHOTOZYME #ERCAdg project, blending #enzymes & #light to craft useful molecules. Grateful to @ERC_research —it's a testament to the work and creativity of past & present young researchers at Melchiorre Group Exciting times ahead! Università di Bologna

Paolo Melchiorre & Melchiorre Group on the Italian news 📺 rainews.it/tgr/piemonte/v… Università di Bologna

The late Nobel Laureate Peter Higgs: "Today I wouldn't get an academic job. I don't think I would be regarded as productive enough." browndailyherald.com/article/2024/0… v Retraction Watch When "publication output" is the holy grail... 1/2

"We fail much more than we ever succeed. We know that. We accept that. We're amazing at dealing with failure. That's what scientists do." - chemist David MacMillan (David MacMillan) on failure at the #NobelPrizeDialogue in Brazil. Watch the full dialogue: bit.ly/3UNzDPa

Important Review on photocatalysis with metals Visible Light-Induced Transition Metal Catalysis | Chemical Reviews pubs.acs.org/doi/10.1021/ac…

nature.com/articles/s4158… Pleased to share our latest work in nature. This paper wraps up our research at ICIQ , and I’m grateful for their incredible support! Looking forward to continuing the journey with the Melchiorre Group Università di Bologna !

Don't miss our last work on the Organocatalytic Asymmetric Electrophilic Amination of Allylic Boronates now out in ACS Catalysis. pubs.acs.org/doi/10.1021/ac…

We are very happy to share our first work at @UniBo on Chemical Science by Sumitava, Enrico and Hailong 🎉 Congrats! Upon deprotonation and excitation with purple light, 3-substituted 4-hydroxycoumarins can act as single-electron transfer (SET) reductants. pubs.rsc.org/en/content/art…

I am very excited to share my first publication from Università di Bologna at Melchiorre Group. Thank you very much to enrico, hailong and all the group member from unibo and ICIQ. Specially Paolo Melchiorre Giorgio Bencivenni for constant help and support.

Exciting opportunity Chemistry Department IIT Madras @BS in Chemistry

🚨 Our first publication is out in J. Am. Chem. Soc.! We uncover how Metal–Arene π-complexation enables selective C–H borylation of polyaromatic compounds. with Bunescu Lab Kavin Raj Kumar Huge thanks to our team and collaborators! 🙌 Please check it out: pubs.acs.org/doi/10.1021/ja…

It is now in Chemistry World magazine (Royal Society of Chemistry). Cascade reaction brings a new dimension to amine synthesis: chemistryworld.com/news/cascade-r…

Congratulations to Ryan and Moto on the publication of their 1,2-acyl transposition in 2,3-dihdyrobenzofurans in Science! science.org/doi/10.1126/sc…

🚀 Cyclopropanes go metal-free! A highly enantioselective cyclopropanation of olefins using diazoalkanes via #ACPC Nature Catalysis No metals, just radical cations & serious selectivity #organocatalysis #asymmetricsynthesis #chemtwitter nature.com/articles/s4192…

Thrilled to share our collaborative work with Prof. Yoonsu Park’s group published in Nature Communications: Superacid counteranion as flexible-coordinating ligand for asymmetric organo-bismuth catalysis. Congratulations to Jin Hyun and Seok Yeol! doi.org/10.1038/s41467…

[1.1.1]Propellane acts as a carbene source in a [2,3]-sigmatropic shift—makes MCBs & leads to benzene-like BCHs via radical cyclization!｜[2,3]-Sigmatropic rearrangement with [1.1.1]propellane nature.com/articles/s4146…

Looking for a cost-effective and efficient organic photocatalyst? Check this one out! 🔬✨ #Photocatalysis #OrganicChemistry #Organocatalysis #SustainableChemistry #GreenChemistry #unibo onlinelibrary.wiley.com/doi/10.1002/an…

I am very happy to share my recent work from Melchiorre Group Università di Bologna in Angewandte Chemie. A bifunctional organic photocatalyst for efficient SET & EnT! 💡 🌱 I deeply appreciate Prof. Paolo, Hailong, Nunzio, Bixiao, Prof. Stefano, Marie Skłodowska-Curie Actions European Commission onlinelibrary.wiley.com/doi/full/10.10…

Today in Science Magazine, we report a method to replace the C2 of pyridines with N, affording pyridazines. The change from electronically consonant (pyridine) to dissonant (pyridazine) opens retrosyntheses not typically available to the latter. science.org/doi/10.1126/sc…