Excited to share our new publication in @J_A_C_S, wherein formal carbonyl insertion was achieved at the para or ortho position of pyridines, enabling access to 1,4- or 1,2-azepinones, which could be smoothly downstreamed into bicyclic pyrrolidinones. https://t.co/6tJtWm8R3K
Excited to share our new publication in @J_A_C_S, wherein formal carbonyl insertion was achieved at the para or ortho position of pyridines, enabling access to 1,4- or 1,2-azepinones, which could be smoothly downstreamed into bicyclic pyrrolidinones. https://t.co/6tJtWm8R3K
Divergent Skeletal Editing of Pyridinium Salts to Azepinones and Pyrrolidinones via Formal Carbonyl Insertion | Journal of the American Chemical Society https://t.co/gM8nLeYNou
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Excited to share our latest work is now out on @J_A_C_S !!!!
We report a visible-light-driven platform for alkyl radical generation from redox-inert substrates based on photo-active sulfur-intermediates formed via polar activation.
https://t.co/4wMM3haOXD
One-Step-Three-Ring Propellanation Reaction of Yne-Vinylcyclobutanones Catalyzed by Nickel: Reaction Development, Mechanism, and Formal Synthesis of Modhephene | Journal of the American Chemical Society https://t.co/WSlEZhZsLF
Excited to share that our pyridine → aniline skeletal editing work is now a Cover Feature in ChemistryEurope. Thanks to everyone for the support!
Free to read: https://t.co/xc8QoXvo0T
Indeed, No Need for HMPA! A DFT Study Comparing the Lewis Basicity of Phosphoric Acid Triamides by Luca Steiner, Hans-Ulrich Reissig, and co-workers (Freie Universität Berlin) #OpenAccess
https://t.co/qabaFbdWQ7
🚀Our pyridine → aniline #SkeletalEditing paper is now #1 Most Accessed article (past 3 months) in @ChemistryEur
📈 Over 1,000+ full-text views in just 20 days. A huge thanks to the community for the incredible interest and support!
🔗 Free to read:
https://t.co/xc8QoXvo0T
Skeletal Editing from Pyridine to Aniline via C-Insertion and N-Isomerization by Yun Luo, Jing Dai, Yongchang Wei, and Chang Min (Wuhan University) #OpenAccess 🔓 https://t.co/1J63lZs2rO
💡Powered by our pyridine-to-aniline skeletal editing, drug candidate Rogletimide can be directly converted into the approved💊Aminoglutethimide—a therapy for Cushing’s syndrome.
#SkeletalEditing accelerates #DrugDiscovery process.
🔗Free to read:
https://t.co/xc8QoXuQbl
One-Step #SkeletalEditing: Pyridine → Aniline
500+ Full Views in first 10 days📈
Featured in "Editor's Choice"
Huge thanks to my advisor Chang Min.
Thank @ChemistryEur@ChemEurope@angew_chem
for sharing our work!
🔗Free to read link in the first reply below 👇
A powerful example: using our pyridine-to-aniline skeletal editing, the drug candidate Glutethimide can be directly converted into the approved 💊 Aminoglutethimide—a therapy for Cushing’s syndrome. #DrugDiscovery
Skeletal editing accelerates drug discovery process.
Skeletal Editing from Pyridine to Aniline via C-Insertion and N-Isomerization by Yun Luo, Jing Dai, Yongchang Wei, and Chang Min (Wuhan University) #OpenAccess 🔓 https://t.co/1J63lZs2rO
Our new paper is out now in @ChemistryEur. In this work, we introduce a sequential Carbon-insertion and Nitrogen-externalization strategy enabling the pyridine-to-aniline conversion in one single step.
#SkeletalEditing#OrganicChemistry
https://t.co/A37mhbAwWX