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pubs.acs.org/doi/10.1021/ac…

A new paper from Derek Sprayberry Aspacio et al. establishes a metabolic system of engineered biocatalysts using the noncanonical cofactor NMN+ for biomanufacturing in cell-free systems and in E. coli without interference from NAD(H) and NADP(H). Read it here rdcu.be/dQPUp

A 4-year PhD studentship in catalysis and synthetic organic chemistry, to start in January 2025 or later, is available in my group Durham Chemistry! 🇬🇧, 🇪🇺 and 🗺️ candidates all welcomed to apply by 27/09/24. Info and how to apply: tinyurl.com/yhjepb9k

How do you turn a deletion into an insertion? In our latest, Myojeong shows that the anomeric amide can N-delete *and* re-aminate a sulfinate intermediate, enabling an overall SO2 insertion. Another great collab with Christopher Kelly and J&J! doi.org/10.26434/chemr…

Oxygen walking seems pretty sweet to access these C-3 oxygenated pyridines. It's also pretty cool to see the formation of a Dewar-type lactam from the C-2 byproduct. Another banger from the Qin group. pubs.acs.org/doi/10.1021/ja…

onlinelibrary.wiley.com/doi/10.1002/an…

The final version of this study on the discovery and mechanistic elucidation of an unusual anti-cyclopropanation rxn is now online J. Am. Chem. Soc.. A great collaboration w/ Peng Liu Group, Piercey lab Purdue Energetics Research Center, and #PfizerChemistry led by Huiqi Ni. tinyurl.com/3hmpjp4k

Scientists should get paid for thinking time nature #PhD #PhDlife #academics #AcademicChatter #AcademicTwitter #Postdocs #Research #Science

Thrilled to share the first Palkowitz lab paper with you all! While the reaction is simply a Buchwald, the synthetic hole in the literature it fills is made clear by comparison to prior routes towards accessing these important cereblon binding motifs! chemrxiv.org/engage/chemrxi…

Do you think Suzuki-Miyaura coupling always requires the presence of a base? No! Check out our newest publication about the SMC of aryl thianthrenium salts under acidic conditions! Out now in Nature Synthesis! rdcu.be/dR0sc Congrats to all involved!

Skeletal editing: Nitrogen-to-Functionalized Carbon Atom Transmutation of Pyridine Just published in Chemical Science by Glorius Group in collaboration with Osvaldo OG_labs👏👏 pubs.rsc.org/en/Content/Art…

Here is our latest publication in the field of #Halotriarylbismuthonium salts. Impressive to see the differences between Cl and F.🤓 Great work with Cornellab, Jennifer Kuziola and Markus L. pubs.rsc.org/en/content/art…

Our work on isolable Ni-Alkyl complexes for alkyl-alkyl cross-coupling reactions is now out in nature! Scope, mechanism, and more in another great collaboration with Dipa Kalyani and Merck. Congratulations to the entire team! nature.com/articles/s4158…

By harnessing the power of organobismuth compounds, the Viresh Rawal group have developed a sustainable, efficient & metal-free method to create arylethylamines—essential building blocks in many drugs. Li Li Chem UChiPhysicalSciences cell.com/chem/abstract/…

Activation and Catalytic Degradation of SF6 and PhSF5 at a Bismuth Center | Journal of the American Chemical Society Cornellab #SF6 #PhSF5 #Bismuth pubs.acs.org/doi/10.1021/ja…

📣 The latest ERC Starting Grant competition results are out! 📣 494 bright minds awarded €780 million to fund research ideas at the frontiers of science. Find out who, where & why 👉 europa.eu/!hrxyBp 🇪🇺 #EUfunded #FrontierResearch #ERCStG Horizon Europe🇪🇺 EUScience&Innovation🇪🇺

⭐️ Nova axuda #ERCStG para a USC, dirixida a combater a resistencia aos antibióticos. 🚀 O Dr. Nacho Insua consegue o respaldo do prestixioso programa europeo European Research Council que impulsa a investigación de vangarda apoiando a mozos investigadores no

Extremely happy to share that we have been awarded an ERC StG from European Research Council (ERC) ! Exciting times ahead for the group pursuing our ideas in PCET and catalysis with #More4Less project!

Unified Method for Oxidative & Reductive Decarboxylative Arylation with Orange Light Ir/Ni Metallaphotoredox Catalysis | JACS Columbia University Columbia Chemistry Rovis Group Total Synthesis and Methodology Highlights #Oxidative #Reductive #Decarboxylative #Arylation #Ir #Ni #Metallaphotoredox pubs.acs.org/doi/10.1021/ja…

Zn and Mn are commonly used reductants in organic chemistry - but what are their redox potentials in organic solvent?!? Zhiming and Ruohan provide an answer and show why it matters in Ni XEC reactions. UW-Madison Chemistry Nature Chemistry (full access link) rdcu.be/dTa4I