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Join us in congratulating Nikita and Valeriia for discovering a new reactivity of diazo compounds, undergoing branch-selective hydroalkylation with alkenes. Initial findings suggest a carbene-type mechanism which is unusual for nickel catalysis. Published today in J. Am. Chem. Soc.

Asymmetric Hofmann–Löffler–Freytag-type reaction via a transient carbenium ion complex merging organocatalysis and photocatalysis bit.ly/4iCBNLi

Congratulations to Ryan and Moto on the publication of their 1,2-acyl transposition in 2,3-dihdyrobenzofurans in Science! science.org/doi/10.1126/sc…

Organocatalytic regio- and stereoselective cyclopropanation of olefins bit.ly/3GTSd5b

We are excited to share our new work on one carbon alkene homologation. We can iteratively homologate terminal and internal alkenes in simple and complex molecules using this method. Great work by Marcus that opens up lots of exciting opportunities for us. nature.com/articles/s4158…

Excited to share that our one-carbon alkene homologation reaction developed Marcus Grocott by has been published in @nature🎉 doi.org/10.1038/s41586… (1/3) 🧵

We are hiring! Postdoctoral positions are available in the field of(1) skeletal editing and (2) autonomous organic synthesis. RT appreciated 🙏 Check out our recent contributions, published in Science (2024): Photocatalytic Furan-to-pyrrole conversion, science.org/stoken/author-…

Along with the Top 200 Drugs of 2024, the Njardarson lab has also released the Top 200 Small Molecule Drugs of 2024! Free high res download at the link below. bpb-us-e2.wpmucdn.com/sites.arizona.…

Profs. Hong and Lee at SNU unveil a cooperative catalytic system using organosulfur shuttling to enable inner-sphere C(sp³)–N coupling—bypassing redox limits for late-stage access to complex arylamines. doi.org/10.1021/jacs.5… #RadicalChemistry #Photoredox #OrganosulfurCatalysis

Iridium-Catalyzed Nitrene-Mediated Enantioselective 1,2-Hydride Shift Enabled by Attractive Noncovalent Interactions for Chiral δ-Lactam Synthesis | Journal of the American Chemical Society Total Synthesis and Methodology Highlights pubs.acs.org/doi/10.1021/ja…

🚨 A single-atom swap could change the game in drug discovery! 🧪💥 We have just unveiled a CO-to-S atom swap method that turns ketones into sulfur-containing frameworks in complex, bioactive molecules in just two steps. science.org/doi/10.1126/sc… Congratulations to Zining.

Online now: Catalytic and selective chemical recycling of post-consumer rubbers into cycloalkenes dlvr.it/TLQwq3

We're hiring postdocs! Fully funded positions in catalysis & stereoselective synthesis, organometallic chemistry. Learn more at our group website (cataleesis.kaist.ac.kr). Interested? Send your CV to [email protected] — we’ll follow up with additional documents (e.g.

The Glorius Group is calling for a passionate postdoc who wants to shape the future of digital chemistry – where ML models, mass spectrometry, and human insight meet. ⚗️💻😀 In collaboration with: lab25, ChemInnovation 🚀 🙏 RT #chemistry Jobposting: stellen.uni-muenster.de/jobposting/4e9…

Visible Light Promotes PIII/PV-Catalyzed Reductive N-Arylation of Nitroarenes at Room Temperature | ACS Catalysis pubs.acs.org/doi/10.1021/ac…

Our third project on alkene hydrofluorination is now published in JOC (J Org Chem/Org Lett )! We showcase the use of diverse nucleophilic fluorine sources for the synthesis of β-fluorinated amides. Congrats to Baeho and Dohyun! pubs.acs.org/doi/10.1021/ac…

Grateful to share that my third asymmetric version from my PhD journey on C–N bond formation has just been published ASAP in JACS🎉 Many thanks to my collaborators for their great teamwork! J. Am. Chem. Soc. KAIST Chemistry Università di Pavia pubs.acs.org/doi/10.1021/ja…