Impressive design. Congratulations.

🐱 📦 💕

Lol, who made this?

Editing Tetrasubstituted Carbon: Dual C–O Bond Functionalization of Alcohols Enabled by Pd-Based Dyotropic Rearrangement | JACS Zhu Group EPFL Chemistry Total Synthesis and Methodology Highlights #Editing #TetrasubstitutedCarbon #COFunctionalization #Dyotropic #Pd #Rearrangement pubs.acs.org/doi/10.1021/ja…

nature.com/articles/s4155… Interesting transformation from JP Lumb , the “hydroxyl migration” of para-phenols

Discovery, Characterization, and Synthetic Application of a Promiscuous Nonheme Iron #Biocatalyst with Dual Hydroxylase-Desaturase Activity by Hao Xu, Jidong Zhao, and Hans Renata Hans Renata at Rice University Chemistry Department in ChemRxiv chemrxiv.org/engage/chemrxi…

Unexpected Transformations during Pyrroloiminoquinone #Biosynthesis by Josseline Ramos-Figueroa, Lingyang Zhu, and Wilfred A. van der Donk at Chemistry at Illinois in J. Am. Chem. Soc. pubs.acs.org/doi/10.1021/ja…

Congrats @yannickbraegger, Ann-Sophie K. Paschke, Nima Nasiri, Bence B. Botlik and Francesco Felician for this masterpiece! Oxidative amination of unactivated alkenes via nitrogen atom insertion into carbon-carbon double bonds. ChemRxiv - go.shr.lc/3UQNC6L

Check out our newest paper on the Alcohol-Directed Aliphatic C-H Functionalization. Congrats Dom! pubs.acs.org/doi/full/10.10…

Check out this tour de force led by @sbuzsaki Rice University Chemistry Department and Savannah Mason Yale Chemistry in collaboration with Miller Group and Pat Holland! The first asymmetric radical hydrogenation with some mechanistic surprises along the way! #realtimechem

Thrilled to share our latest work in nature in collaboration with the Davis Group at Rosalind Franklin Institute & Oxford Chemistry. We developed a 'cap & glycosylate' strategy that directly transforms native sugars into glycosides & glycoproteins! NUS Chemistry #glycotime nature.com/articles/s4158…

We are excited to announce that Guangbin Dong has won the 2024 Mitsui Chemicals Catalysis Science Award. The highly prestigious award honors contributions to the sustainable development of chemistry in catalysis science The Dong Lab UChiPhysicalSciences UChicago Pritzker School of Molecular Engineering chemistry.uchicago.edu/news/guangbin-…

Congrats Guangbin, well deserved.

Skeletal Editing of Cyclic Molecules Using Nitrenes SUSTech 南方科技大学 doi.org/10.1002/cjoc.2…

Exciting news!🎉 Our paper about the selective reduction of esters to aldehydes is currently the most read article in J. Am. Chem. Soc. with over 12,000 reads in just two weeks! Huge thanks for the great feedback! Stay tuned for more exciting FLP chemistry soon! pubs.acs.org/action/showMos…

🚨RADICAL RETHINK: STEREORETENTIVE CROSS COUPLING UNLOCKED🚨 Today in ChemRxiv (chemrxiv.org/engage/chemrxi…) 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

Excited to share that “Palladium and Norbornene Cooperative Catalysis: Fundamentals and Applications”—edited by Guangbin—is now available via Wiley! wiley.com/en-sg/Palladiu…

Our in-insect nanocarbon synthesis is now out in Science Magazine. Enjoy our crazy campaign feeding molecules to insects densely packed with diverse enzymes and let them produce new functional compounds! Many thanks and huge congrats to all involved!! science.org/doi/10.1126/sc…

… and another one this week from the Knowles Lab, “Ring Expansions of 1,2-Amino Alcohols to Amine Heterocycles Enabled by Proton-Coupled Electron Transfer,” in J. Am. Chem. Soc.. Nice work Danny and Rob: doi.org/10.1021/jacs.5…

Reactivity of alkenyl pyrazole species.