PG Echeverria
@PGE13
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🚀 #SynTech2026 – Save the Date! 📅 6–8 July 2026 | Old Royal Naval College, London 🇬🇧 Join us for the 1st SynTech Summer School & Conference: electrosynthesis, flow, photochemistry, AI & more! Pre-register 👇 https://t.co/tDlGgUNsq7
#RealTimeChem
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Glad to buy this beautiful book about Ryoji Noyori one of my chemistry heroes during my PhD! @livesinchem
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Mechanism of Redox-Neutral Radical Cross Coupling (another fun collaboration with the Blackmond Group), out today in @ChemRxiv : https://t.co/OD6HK6HTiY
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Terpenoid Synthesis via Convergent Radical Annulation! Appearing in @ChemRxiv today: https://t.co/YJnIp0FJ3Z
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I am glad to share this debenzylation method published in @OPRD_ACS Great work performed with great team! https://t.co/dP6hMTZsSH
pubs.acs.org
Benzyl-protected amines are mainly deprotected on scale using palladium-catalyzed hydrogenolysis. The present study evaluates a metal and hydrogen-free alternative based on the amine moiety oxidation...
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The first time @BRSM_blog found organic chemistry fascinating was in an undergraduate course on natural products. Amongst stories about beautiful molecules and legendary scientists who jockeyed to understand and eventually make them, he was hooked. https://t.co/LmJNtfS3qF
chemistryworld.com
A stepping stone to greater things?
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Appearing today in @Nature :
nature.com
Nature - Readily accessible enantioenriched sulfonylhydrazides and low loadings of an inexpensive achiral Ni catalyst can be used to control the stereochemical outcome of radical cross-coupling.
🚨RADICAL RETHINK: STEREORETENTIVE CROSS COUPLING UNLOCKED🚨 Today in @ChemRxiv ( https://t.co/UixXSDpA2R) the first method for stereoretentive radical cross-coupling is disclosed. No fancy ligands or redox needed—just a Ni-diazene twist. 120 years after Gomberg, a new chapter
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Happy to share this work on electrochemical alpha-functionalization. A great joint efforts with @SamerGnaim & @Julien07
https://t.co/jPN5zjXdXG
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TEN STEPS TO A MARINE TREASURE: Gram-Scale Synthesis of Bipinnatin J – featuring methods that weren't known ≅3 years ago to forge 3 key C–C bonds... Appearing today in @ChemRxiv ( https://t.co/mJBAdPz7Jd). Quick Summary: A concise, scalable total synthesis of (–)-Bipinnatin J
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🚨RADICAL RETHINK: STEREORETENTIVE CROSS COUPLING UNLOCKED🚨 Today in @ChemRxiv ( https://t.co/UixXSDpA2R) the first method for stereoretentive radical cross-coupling is disclosed. No fancy ligands or redox needed—just a Ni-diazene twist. 120 years after Gomberg, a new chapter
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Looking forward to it! Today?
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Appearing today in @ScienceMagazine :
science.org
Sulfonyl hydrazides are stable and usually crystalline substances that can be accessed in a variety of ways, including transiently from hydrazones, to achieve a net reductive arylation of carbonyl...
Finally, RADICAL CROSS COUPLING without the exogenous REDOX. We disclose in @ChemRxiv ( https://t.co/C4auh5reyl) a broadly general platform for achieving transformations that normally required excess metallic or chemical reducing agents or photochemical setups (and their
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⚡ Crash course in modern echem out now! Here, we learn about echem against the back drop of modern case studies!⚡️ Thank you @MatthewHorwitz1 and the rest of the team at Synthesis Workshop for the invitation! https://t.co/yDP9ITbPyd
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SAXITOXIN simplified: Appearing today in @ChemRxiv is a short, highly scalable, convergent approach to this entire natural product family using a tactical combination of radical retrosynthesis, biocatalysis (in collaboration with Merck), and C–H functionalization logic:
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Scholarly review written by @DirkTrauner and @GloriusGroup: Reaction development: a student's checklist📜☑️😀 Published in Chem. Soc. Rev.: https://t.co/FnzvDvrV4b
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[#ExOL] 15 janvier 2005 : « Si je suis là, c'est pour prendre vos places ! » Mission plus qu'accomplie ! Il est parti devant et personne ne l'a revu. 😁 20 ans de carrière aujourd'hui ! 🎂 Joyeux anniversaire @Benzema ! 🫡⚒️ #TeamOL #Nueve #Ballondor
https://t.co/QcZIelGkOC
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⚡️Electrosynthesis scale up alert! ⚡️Happy to share our @OPRD_ACS article detailing lessons learned on improving robustness of electrosynthesis setups across scales. #MerckChemistry
https://t.co/hqjnXlCNNt
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📢Call for Papers: Lessons Learned in Organic Process Chemistry Submissions due April 2025 Share your experience in overcoming negative outcomes and unexpected results with the organic chemist community. Learn more about the scope of the Special Issue: https://t.co/dMob8Dx1Tj
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Pyrolytic Carbon: An Inexpensive, Robust, and Versatile Electrode for Synthetic Organic Electrochemistry (Phil S. Baran and co-workers) @BaranLabReads @yukawamata @chemistte
onlinelibrary.wiley.com
Synthetic organic electrochemistry is a highly useful redox method, enabling diverse transformations. This study explores pyrolytic carbon electrodes in powerful rAP processes and C−C as well as C−N...
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