#skeletalediting #expansion #electrochemistry #heterocycle
Article by Yu Zhao, Ming Joo Koh & co-workers
Divergent synthesis of N heterocycles from carbocycles enabled by electrochemical nitrogen atom insertion
www.nature.com/articles/s44... ($)
#Chemsky
#skeletalediting #expansion #electrochemistry #heterocycle
#UChicago #UChiChemistry #JanssenPrize #OrganicSynthesis #GuangbinDong #SkeletalEditing #Chemistry
#UChicago #UChiChemistry #JanssenPrize #OrganicSynthesis #GuangbinDong #SkeletalEditing #Chemistry
👉 buff.ly/XvYGfsW
👉 buff.ly/XvYGfsW
Nice to see a cool write up about cutting edge synthesis in the media
Nice to see a cool write up about cutting edge synthesis in the media
“ #CE&Nuncovered The Strange Copy & Paste #Chemistry of #SkeletalEditing” @cenmag.bsky.social
🧪
podcasts.apple.com/us/podcast/s...
“ #CE&Nuncovered The Strange Copy & Paste #Chemistry of #SkeletalEditing” @cenmag.bsky.social
🧪
podcasts.apple.com/us/podcast/s...
Twofold 4-to-6 ring expansion of azetines to bis-halogenated pyridines
🔗 doi.org/10.1039/d6qo...
#SkeletalEditing #RingExpansion #Pyridines #CarbeneChemistry #OrganicSynthesis #Heterocycles
Twofold 4-to-6 ring expansion of azetines to bis-halogenated pyridines
🔗 doi.org/10.1039/d6qo...
#SkeletalEditing #RingExpansion #Pyridines #CarbeneChemistry #OrganicSynthesis #Heterocycles
Nagoya University went inside anyway, cutting a bond deep inside a flat molecule and rebuilding it.
Out came nanocarbons that emit spiraling light.
#SkeletalEditing #Nanocarbon #Chemistry
Nagoya University went inside anyway, cutting a bond deep inside a flat molecule and rebuilding it.
Out came nanocarbons that emit spiraling light.
#SkeletalEditing #Nanocarbon #Chemistry
Source: https://phys.org/news/2025-05-atom-swapping-method-successfully-complex.html
Source: https://phys.org/news/2025-05-atom-swapping-method-successfully-complex.html
, wherein formal carbonyl insertion was efficiently achieved at the para or ortho position of pyridines, enabling access to 1,4- or 1,2-azepinones, which could be smoothly downstreamed into pyrrolidinones.
Link: doi.org/10.1021/jacs...
#SkeletalEditing
, wherein formal carbonyl insertion was efficiently achieved at the para or ortho position of pyridines, enabling access to 1,4- or 1,2-azepinones, which could be smoothly downstreamed into pyrrolidinones.
Link: doi.org/10.1021/jacs...
#SkeletalEditing