A mild strategy compatible with various solvents, air, and moisture @angew_chem
Congratulations to all involved!
Geminal Difunctionalization of Ketones via C─S Bond Insertion of Photogenerated Donor–Donor Diazo Compounds
https://t.co/yGa1DDOZ3F
🎉 Chuffed to see our JACS paper is among the most read articles this month!
See how a boron-mediated Ni/photoredox strategy for hydroalkylation of olefins enabled the access to quaternary carbons.
https://t.co/rf1HXDopsr
Congrats Team!
#Photoredox#Organoborons@BristolChem
Our dual photocatalytic method enables the selective synthesis of aniline under mild conditions and allows easy scaling with flow systems. Nice team work! @ChemEurJ
https://t.co/pg7vpmlyq4
Our perspective charts the potential of water as a programmable reaction medium using compatible catalysts, EDA complexes, engineered micelles and microdroplets. Congrats @yaming_tian
Aqueous-phase organic photochemistry: Distinct modes and interfaces
https://t.co/jOqPZJffYD
⚡Electrons as reagents 🔋! Strained rings undergo programmable ring opening, merging C–C & C–H activation for divergent, multi-functionalized scaffolds—strain meets electrochemistry in full control mode 💥🧪
@NatureChemistry
https://t.co/IrRCGNP19W
New in Angewandte Chemie International Edition 🎉
1st corresponding author paper from Australia | 3rd Angewandte
NIR photocatalysis—an emerging field, now with a focused minireview.
Dedicated to Dilip D. Dhavale (SPPU, India) 🙏
https://t.co/PurzwMhUfr
As part of the new 'Photoredox Catalysis' special issue, we present our account on the use of thianthrenium salts in photochemistry! SET, energy transfer and photoinduced homolytic cleavage – thianthrenium salts can do it all!
Open access🔓
https://t.co/QmGVTVOcoB
🦋Remodelling of BCB: Our work on skeletal remodelling of BCBs to all‑carbon quaternary oxindoles via a deconstruction and reconstruction approach is out @ChemRxiv. Thank you, @iiscbangalore@ANRFIndia, for the financial support.
https://t.co/8hQMO2hqQG
'On Water' hydrogen bonding stabilizes the photo-excited state of quinones: application of Franck-Condon principle in organic synthesis.@NatureComms
Congrats to all!
https://t.co/uQGknuV7CI
“On-water” photosensitization enables redox neutral acylation and alkylation of quinones
We broadened the scope of 4-isoxazolines and oxa-aza-BCHeps in a highly regioselective fashion by photocontrol over strain and topology. A template for designing next-generation therapeutics and agrochemicals!
https://t.co/6P1Z0wUjh9
🦋 Photocontrol over strain and topology: divergent nitrone [3+2] cycloadditions with BCB deliver isoxazolines or oxa-aza-bicycloheptanes, redefining exit from flatland ⚡🔺
@ChemistryKoenig@ChemRxiv
https://t.co/m8ThCfAuTW
A ring-open–close programmability
Photocatalytic Reconstruction of Bicyclo[1.1.0]butanes to Oxygenated Bicycles | Journal of the American Chemical Society https://t.co/oY28nwkKeF
A versatile route to sulfur analogs of beta-lactams: efficient, broad scope, advanced to sulfonamides by energy transfer catalysis @scie|https://t.co/bYfDDdRtSL