This is an exciting opportunity for an industry focussed PhD in flow chemistry and catalysis. In partnership with our lab, CSIRO and Precision Catalysts. Please see the link below for details! Catalytic Static Mixers in Organic Synthesis. research.csiro.au/iphd-opportuni…

⚡️Open Postdoc Position⚡️ We are hiring a postdoc in electroorganic synthesis with 3d transition metal catalysis. The position starts on September 1 or October 1. Applications are due by July 18. Please see details: choi.cbnu.ac.kr #Chempostdoc #Chemtwitter @chemjobber

Special day for our group today. Our first undergraduate students Μιχάλης and @paraskevipap03 presented their diploma thesis. Congratulations I wish you all the best in your future endeavours.

Our lab started a new activity #ClassicsFriday! We’re going through Classics in Total Synthesis (Nicolaou and Sorensen) chapter by chapter. This week we discussed Corey’s groundbreaking synthesis of the Prostaglandins (1969): pubs.acs.org/doi/10.1021/ja… What’s your favorite classic

Excited to share this new primer on Flow Chemistry! Learn the foundations of flow synthesis in collaboration with ⁦Duncan Browne⁩ ⁦Anna Slater (she/her)⁩ and ⁦Baumann Research Group⁩ ⁦⁦Nature Reviews Methods Primers⁩ nature.com/articles/s4358…

Modular, scalable, & safe access to α,α-difluoromethylene amines (NCF₂R) using flow chemistry! Three diversification points, mild conditions, & broad functional group tolerance. Check it out ChemRxiv! 📄 chemrxiv.org/engage/chemrxi… #FluorineChemistry #FlowChemistry

Cracking one of synthesis’s toughest nuts: dioxygen activation! In collaboration with the Costas Lab Miquel Costas , our DKP-Mn combo hits selective C–H oxidation of alkanes with sharp chemoselectivity under aerobic conditions. Many congrats Kiki! pubs.acs.org/doi/10.1021/ja…

Out today in J. Am. Chem. Soc. is the first synthesis from our group!! We report a convergent and stereoselective total synthesis of the nominal structure of Talaromyolide D. Huge congrats to Bo and Alex! NYU Chemistry Total Synthesis pubs.acs.org/doi/10.1021/ja…

Our latest in J. Am. Chem. Soc., we report a general strategy to access antimicrobial sactipeptides by Markovnikov hydrothiolation of dehydroamino acids. Congratulations to Yiwei, Shuvendu, Steven and Yannik for their hard work! pubs.acs.org/doi/10.1021/ja…

Just accepted!! Many congrats Kalliopi! pubs.rsc.org/en/content/art…

3 weeks left!!! ΠΡΟΣΚΛΗΣΗ ΕΚΔΗΛΩΣΗΣ ΕΝΔΙΑΦΕΡΟΝΤΟΣ ΜΕΤΑΠΤΥΧΙΑΚΟΥ ΠΡΟΓΡΑΜΜΑΤΟΣ “ΚΑΤΑΛΥΣΗ-ΠΡΑΣΙΝΗ ΧΗΜΕΙΑ ΚΑΙ ΕΦΑΡΜΟΓΕΣ ΤΟΥΣ ΣΤΗ ΒΙΟΜΗΧΑΝΙΑ" ΑΚΑΔ. ΕΤΟΥΣ 2025-26 Περισσότερες πληροφορίες: chem.uoa.gr/anakoinoseis_k…

Looking for a green, mechanochemical shortcut to 4-hydroxy-2-pyridones from tetramic acids—biosynthesis-style? We’ve got you covered. Check out our latest in Green Chem! 👏 Huge congrats to Kalliopi for leading the charge! pubs.rsc.org/en/content/art…

Glad to share our recent #JOrgChem article on catalytic asymmetric Total Synthesis of naturally occurring Amaryllidaceae alkaloids, (−)-elwesine and (−)-epi-crinine! Congratulations to Satyajit Majumder Debabrata Mondal Abhishek Mondal Souvik Pal👏 pubs.acs.org/doi/10.1021/ac…

We built a machine learning–guided workflow to optimize reaction conditions for photochemical nickel-catalyzed cysteine arylation; no specialized robots or fancy HTE plates needed! Check it out ChemRxiv: chemrxiv.org/engage/chemrxi… #MachineLearning #ReactionOptimization

In Nature Synthesis, we provide our perspective on the blossoming of organo-TT chemistry since 2019. From fundamentals to applications, we explain how the thianthrenium substituent enables chemistry that in part goes beyond that of other (pseudo)halides. rdcu.be/eIEM6

Interested in cutting strong bonds in the presence of weak ones? Check out what Mn(PDP) catalysis can do when you change it’s mechanism of action nature (Advanced Article Preview) : nature.com/articles/s4158…

Excited to share that we have received the Hansen Family Award: Groundbreaking Research: Chemist Lutz Ackermann Receives Bayer Foundation’s Hansen Family Award | Bayer Foundation ⁦Uni Göttingen⁩ bayer-foundation.com/groundbreaking…

📢 We are recruiting PhD candidates to join our dynamic research group at Uni of Nottingham #WeAreUoN ! ⚗️🧪🧑‍🔬👩‍🔬💡 Check out our website silviresearch.com for more info and to find out how to apply! 👀

We just achieved the first site-selective cysteine functionalization with EBX reagents! J. Am. Chem. Soc. pubs.acs.org/doi/10.1021/ja…

⚡️We are happy to share our recent work in Angewandte Chemie with a collaboration with Kim group at CNU. By adjusting electrochemical conditions, we access haliranium-mediated C–O bond or amidyl-radical-driven C–N bond formation, supported by CV, kinetic, and computational studies.