@SCORE_Lab_Lyon

Discovering, developing and understanding new catalytic tools and synthetic methodologies in organic chemistry.

 ICBMS Lyon
Joined February 2022
  • Tweets220
  • Following217
  • Followers558
30Media
SCORE Lab retweeted
Masson Group@GroupMassonFeb 13
From design to mechanism: Masson Group introduces tunable triaryl-heptazines as high-potential photoredox catalysts for selective oxidative transformations. pubs.acs.org/doi/10.1021/acs…

Triaryl-Heptazine Photocatalysts for the Oxidation of C–H and C–C Bonds in Nitrogen-Containing...

Abstract. Open-shell intermediates have become central to modern organic synthesis, placing photoredox catalysis, and therefore the development of photocat

pubs.acs.org
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Radical Retrosynthesis of Natural Products Enabled by Iron-based Reductive Olefin Coupling. Published today in @ChemRxiv : chemrxiv.org/engage/chemrxiv…
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Editorial: Photocatalysis for Sustainable Energy dx.doi.org/10.1021/acsaem.5c…

Editorial: Photocatalysis for Sustainable Energy

By directly converting solar energy into chemical transformations, photocatalysis represents a promising route toward achieving carbon neutrality and addre

pubs.acs.org
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Alder-Ene strain-release pericyclic cascade reactions of BCBs ⚡️⚡️⚡️Regio- and Diastereoselective Cascade Reactions of Bicyclo[1.1.0]butanes: Access to gem-Difluorinated Carbocyclic Rings | Organic Letters pubs.acs.org/doi/10.1021/acs…

Regio- and Diastereoselective Cascade Reactions of Bicyclo[1.1.0]butanes: Access to gem-Difluorin...

Abstract. gem-Difluorinated carbocyclic rings are attractive motifs in drug development. Herein, we report the transition-metal free cascade reaction of bi

pubs.acs.org
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We are very happy to share our first work at @UniBo on @ChemicalScience 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/arti…
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📢 We are hiring‼️ One #postdoctoral position available in the supramolecular electrochemistry and electrosynthesis. Don't miss the opportunity to join us! Check details👇 and please RT! @eMOCA_IPCM @IPCM_Sorbonne #electrochem #AcademicTwitter #postdocjobs #chemtwitter
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Congratulations to @h_maashi, Abdulrahman, Kharou, Michael, James and Ethan whose work on electrochemical deconstructive heterocycle synthesis has been published in Org. Lett @JOC_OL @ChemistryCU @BathChem pubs.acs.org/doi/10.1021/acs…
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Happy to be back at @ICBMSLyon for the Journées Victor Grignard. @JeremyMerad on stage talking about most of my PhD work and subsequent projects in @SCORE_Lab_Lyon
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Less than 2 weeks to apply for a PhD position in ⁦@KLEIJ_ICIQ⁩ laboratory ⁦@ICIQchem⁩! Focus will be on TM cat #stereoselective #synthesis. Only ONLINE apps are evaluated 📺, who wants to invest 4 y in groundbreaking research 🔬? RTs 🙏 👍 careers.iciq.org/jobs/476557…
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Our spinoff company Linium Biochemicals (liniumbio.com/) is looking for two highly skilled chemists (permanent position, PhD level) to tackle the challenge of lignin depolymerization. A fantastic project in a brand new lab with a fun team in Paris area. Please RT
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Chiral amino alcohols without the hassle, radically simplified appearing today in @ChemRxiv : chemrxiv.org/engage/chemrxiv…
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A post-doctoral position in electrosynthesis, organometallic and @Boron_Chemistry (funded by @UNamur "BatFactory" 🇪🇺🇧🇪project) is available in the group. Applications until January 15ᵗʰ 2024 🗓️. 🔽See details below.⬇️ Please RT✔️.
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Electroreductive Synthesis of Nickel(0) Complexes (Keary M. Engle and co-workers) @EngleLab @BaranLabReads @Julien07 @CamZRub @g_laudadio @chemistte #openaccess onlinelibrary.wiley.com/doi/…

Electroreductive Synthesis of Nickel(0) Complexes **

An electrochemical reduction of Ni(II) salts to make Ni(COD)2 on preparative scales is reported. The method was extended to other useful precatalyst complexes such as Ni(COD)(DQ), Ni(tBustb)3,...

onlinelibrary.wiley.com
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Electrochemical Nickel-Catalyzed Selective Inter- and Intramolecular Arylations of Cysteine-Containing Peptides (Samir Messaoudi and co-workers) @samuccen @CNRSchimie @BioCIS @UnivParisSaclay #openaccess onlinelibrary.wiley.com/doi/…

Electrochemical Nickel‐Catalyzed Selective Inter‐ and Intramolecular Arylations of Cysteine‐Conta...

A practical electrochemical Ni-catalytic system has been developed for selective (hetero)arylation, alkenylation and alkynylation of cysteine-containing peptides. The high functional group compatib...

onlinelibrary.wiley.com
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Exploiting the Limits of Divergency Scaffolds in Natural Product Synthesis: The Case Study of Sesquiterpenoids | ChemRxiv - go.shr.lc/46gCDrc Impressive and clever work in total synthesis!!! nice job @zografos_alex

Exploiting the Limits of Divergency Scaffolds in Natural Product Synthesis: The Case Study of...

Divergent synthesis is a powerful but yet underdeveloped method to address the usual drawbacks of poor supply and confined diversity in the total synthesis of natural products. Herein, we describe...

chemrxiv.org
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☺️We are delighted to welcome Prof. Tatiana Besset as our young plenary speaker on Thursday the 7th, at EuCOMC XXV @BessetTatiana @RSEQUIMICA @UAHes @EuChemS @OEuchems congresosalcala.fgua.es/euco…
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We can do blue light, we can do red light—what’s next? Check out our newest paper on C(sp2)-C(sp3) coupling using Iridium and orange light photoredox catalysis! Tis the pumpkin spice latte season y’all! 🎃🍂 @J_A_C_S pubs.acs.org/doi/full/10.102… – at Manhattan, NY

Orange Light-Driven C(sp2)–C(sp3) Cross-Coupling via Spin-Forbidden Ir(III) Metallaphotoredox...

Abstract. We report the development and characterization of a library of Ir­(III) photocatalysts capable of undergoing spin-forbidden excitation (SFE) unde

pubs.acs.org
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Beautiful talk about nickel combining photocat/electrochemistry and organometallic chemistry from my friend @amgoune_abder at the @GECO_Congress !
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We are thrilled to share a new HF-free technology that converts fluorspar to fluorochemicals. Enormous congratulations to the amazing team of chemists who made this recurring dream a reality! science.org/doi/10.1126/scie… @CalumPatel @ScienceMagazine @OxfordChemistry @Fluo_Rok
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Replying to @P_van_de_Weghe @SocietyOfficiel
L'université allemande Friedrich Alexander d'Erlangen (FAU) a décidé de cesser d'accueillir les doctorants chinois financés par le CSC au motif de la protection contre l'espionnage scientifique et industriel, et la sauvegarde de la propriété intellectuelle universityworldnews.com/post…

German university ends ties with China scholarship scheme

A prestigious German university has decided to suspend collaboration with students funded by the China Scholarship Council “to reduce the risk of in...

universityworldnews.com
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