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Check out the new photocatalytic process from the Paixao group (MWPaixão Group) in #OL: Unlocking new reactivities of azomethine imine dipoles through visible-light photoredox catalysis. buff.ly/339Yof2

Here is an infograph showing our short trajectory through the field of visible-light photocatalysis!!! We are proud of how much we could learn  along the path !! Thanks José A. C. Delgado for compiling and preparing this amazing overview !!

Photocatalyzed Intramolecular [2+2] Cycloaddition of N-Alkyl-N-(2-(1-arylvinyl)aryl)cinnamamides (Paixao) José Tiago Menezes Correia, MWPaixão Group, Bianca Matsuo, KoenigChemistry onlinelibrary.wiley.com/doi/10.1002/ch…

We are thrilled to share our recent work on visible-light photoredox catalysis published in Org. Letters (J Org Chem/Org Lett). pubs.acs.org/doi/10.1021/ac… Well done Bianca Matsuo , Pedro_Ramos, and José Tiago Menezes Correia for this beautiful and inspiring work !! PesquisaFapesp , UFSCar #UniversidadeEuDefendo

Complexity and diversity in one shot! We have just published in Chemical Science a new isocyanide-based multicomponent reaction towards the assembly of complex and highly functionalized cyclopentenes !! @FAPESP, UFSCar #UniversidadeEuDefendo

Congratulations to all involved in this beautiful work! Vitor A. Fernandes , Rafaely Lima , Marco Ferreira ⌬ + 💻 + 🇧🇷, Meire Kawamura, Daniel G. Rivera. pubs.rsc.org/en/content/art…

Have you heard yet? Marcio Weber Paixão (Marcio Paixao), SoS ECAB Member, is part of our 3rd Thieme Web #Cheminar🤩 He will report on practical and selective protocols for the preparation of #amide-containing molecules. Register now and learn more 💻👉 fal.cn/3nZs2

Celebrating the review paper on Photoinduced Carbamoylation Reactions: Unlocking New Reactivities Towards Amide Synthesis at RSC-Chemical Communications - pubs.rsc.org/en/content/art…

We are very glad to see that our review "Photoinduced deaminative strategies: Katritsky salts as alkyl radical precursors" is in ChemCommun's top 3% of highly cited articles from the Americas ! 😃🎉

Marcio Paixao, Marco Ferreira ⌬ + 💻 + 🇧🇷 & co. report on a mechanistic investigation of enolate/stabilized vinylogous carbanion-mediated organocatalytic azide (3+2) cycloaddition reactions for the synthesis of 1,2,3-triazoles in our New Talent collection below👇 pubs.rsc.org/en/content/art…

OBC Marcio Paixao Agência FAPESP PesquisaFapesp Ciência UFSCar

Visible-Light Mediated Carbamoylation of Nitrones under a Continuous Flow Regime pubs.acs.org/doi/10.1021/ac…

We are thrilled to share our new contribution for the Synthesis of Non-anomeric C-Glycosyl Pyrazolidinones Derivatives via Visible-Light Photoredox Catalysis. Ciência UFSCar UFSCar #UniversidadeEuDefendo Agência FAPESP PesquisaFapesp Check it out at pubs.rsc.org/en/content/art….

A new strategy for the arylsulfonylation of 2,3-dihydrofuran and vinyl esters in a mild and trans selective manner under Ni and Ru metallaphotoredox catalysis is described! Check it out @ doi.org/10.1002/cctc.2… Ciência UFSCar FAPESP UFSCar #UniversidadeEuDefendo ChemCatChem Martin Group

Be sure to read work in our latest issue by Diogo S. Lüdtke, Marcio Paixao & co MWPaixão Group Ciência UFSCar UFRGS on the synthesis of non-anomeric C-glycosyl pyrazolidinone derivatives via visible-light photoredox catalysis pubs.rsc.org/en/content/art…

Side-Selective Solid-Phase Metallaphotoredox N(in)-Arylation of Peptides | Journal of the American Chemical Society UFSCar #UniversidadeEuDefendo Universität Regensburg Total Synthesis and Methodology Highlights #SiteSelective #Metallaphotoredox #Arylation #Peptides pubs.acs.org/doi/10.1021/ja…

We are thrilled to share our work on metallaphotocatalysis in solid-phase peptide synthesis, focusing on the on-resin orthogonal N-arylation of tryptophan-containing peptides. Congratulations to all the authors!@JoseACDelgado KoenigChemistry Ciência UFSCar PesquisaFapesp

We're thrilled to share our latest article in ACS-OL! In collaboration with Konig's lab, Kim and André have crafted a visible-light-induced, redox-neutral multicomponent reaction for the synthesis of succinamic acid derivatives in good yields. pubs.acs.org/doi/10.1021/ac…