
Leonori Lab
@LeonoriLab
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Group-run account for the Leonori Research Group at RWTH Aachen University. Catalysis. Photoredox. Organic Synthesis.
Aachen, Germany
Joined September 2017
RT @alexandros4285: 🎓A fully funded PhD position in PHOTOCATALYSIS is available in the Ruffoni Research Group at Kiel University. 📝 📩send:….
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RT @n_yasukawa: Checkout the Front Cover Art for our manuscript: "Photocatalytic Strategy for Decyanative Transformations Enabled by Amine-….
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RT @FabioJulia7: If you wonder about how to harness innate excited-state reactivity in TM photocatalysis to design new synthetic methods, y….
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Happy to share our latest results in @angew_chemie on the photochemical permutation of indazoles into benzimidazoles @RWTH .Also, make sure you check a related work from the @SarpongGroup also in @angew_chem .
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RT @alexandros4285: Join our team! We are seeking passionate PDRA and PhD candidates interested in exploring synthetic methodologies and ph….
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RT @synlett_journal: Discover the latest research of Hairong Lyu @HairongLyu and co-workers highlighting the use of a sp²-sp³ #diboron reag….
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RT @Chem_CP: Online now: Excited-state protonation and reduction enables the umpolung Birch reduction of naphthalenes .
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Congratulations to the authors @J_CorpasChem @evariverachao @dr_emarpa @alexandros4285 and the rest of the team including our academic partners and industrial collaborators in Minakem!.
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Our latest publication in @Chem_CP demonstrates the umpolung Birch-like reduction of naphthalenes by photoexcitation employing a very mild acidic solvent (HFIP) and amine-boranes as reductants with high functional group compatibility ⬇️🔗.
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RT @GEMCrisenza: Thrilled to see our first contribution out in @J_A_C_S! @uaitaciano, Roberto, Órla & Ben developed a practical, broad-scop….
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@Nature Well done to Baptiste, @MaialenAlonso8, @GiovanniLonardi, Dilara, Connie, @tds_fm, Yan and @alexandros4285. Thank you also to our collaborators Volker, Maria and Martin from @sanofi and Pep from @JanssenUS.
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@Nature Building on pioneering studies by Pavlik, Maeda, and Vernin, this research demonstrates a way to reconfigure heteroaromatic structures—enabling one ring system to serve as a starting material for synthesizing another.
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Excited to share our latest work on chemical permutation, now published in @Nature! Using photochemical conditions, we've developed a method to selectively and predictably transform the structures of thiazoles, isothiazoles, and other azole systems.
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RT @J_CorpasChem: Check out our most recent work for the synthesis of alkynyl boranes from SOMOphilic alkynes as part of the special issue….
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