@BSadows1@KabiArup@stefano_crespi@UniWarszawski@Boron_Chemistry Nice work! Do you know why the C-I bond cleavage is selective in your case? The use of arylbenziodoxolones has been often limited due to low selectivity in cleavage of one of the two aryl-I bonds...
Check out our newest ChemRxiv preprint on the covalent activation of aryl boronic acids via redox inversion strategy enabled by hypervalent iodine chemistry. Congrats to the team! @KabiArup@stefano_crespi@UniWarszawski@Boron_Chemistry
https://t.co/SrVAGEmzyc
We have an opening for a #postdoc position! Please click on the following link and refer to Advertisement No: IITJ/RD/R/SRP/S/NVT/SDM/20260043/2026/154
https://t.co/vRnyt6PDJI
What we do: https://t.co/HTYGk0TTB3
RTs are appreciated! @SMLab_IITJ@iitjodhpur
Last week at the 8th International Symposium on C–H Activation (ISCHA-8) in Nanjing.
It was a fantastic meeting with inspiring science, stimulating discussions and reconnecting with old friends & meeting new faces.
Delighted to receive a talk award sponsored by @ACSPublications
We are looking for candidates for a PhD position in my group (https://t.co/qGOKcvdXtK) at @UMU to work on new methods for sustainable organic synthesis based on iron photocatalysis.
Deadline: October 1st
More info about the position in the doc below 👇
RT are appreciated!
🦋Radicals and diradicaloids harness the latent energy of strained cycloalkanes, revealing how diradical character and strain release dictate reactivity, selectivity, and molecular complexity 🧪🚀
@J_A_C_S@GargLab@houk1000
https://t.co/TpIJxQ155J
"Strained ring preprint hat trick" at @LcsoLab with the last work of @CarloBalda97 with @IBMResearch@NCCR_Catalysis on the aminoarylation of cyclopropanes using complementary photo- and copper-catalyzed approaches now available at @ChemRxiv
https://t.co/yqawNWlPq3
Triple energy transfer-enabled dearomative cycloaddition/rearrangement cascade of bicyclic azaarenes to structurally complex products https://t.co/oy4IvR18ZE
Check our latest work in @J_A_C_S! We disclose a stereoretentive Yang photocyclization, enabling efficient synthesis of highly substituted cyclobutanols whilst preserving stereochemical information encoded in substrates derived from the chiral pool. https://t.co/LpOcRLzcoE
Just finished a cover to illustrate this paper from @LcsoLab on bicyclobutane transfer reagents!
A smart strategy for making strained BCB scaffolds and accessing sulfur-and carbon-substituted products!
Check it out on @ChemRxiv!
@EPFL_CHEM_Tweet#sciart ⌬ #research ⌬ #chemistry
A convergent access to medium-size rigidified nitrogen heterocycles: Have a look at the last work of Stefano Nicolai and Daphne Lucidarme on the annulation of bicyclobutanes and azadienes to give azabicyclooctanes now as a preprint at @ChemRxiv
https://t.co/495IfbQfrJ
Uphill Photocatalysis with perfect atom economy: Cis-cyclopropanedicarbaldehydes, streamlining access to various drugs. Renewable furans, aldehydes, light, and Lewis acid catalysis are all that is needed. Congrats to Tim and Thomas! https://t.co/wpLmhGOrwH
Bench-stable Ni(II) precats w/ superb solubility that activate cleanly & work ↔️ Suzuki–Miyaura, Buchwald–Hartwig, Miyaura borylation, and olefin difunctionalization. The final version of Nana & Aimee's Ni(C6F5)2 paper is out @Orgmet_ACS#BMSChemistry https://t.co/eUyoYnWL7B
Very happy to introduce BCB-Bx as an electrophilic bicyclobutane synthon!
Have a look at the preprint at @ChemRxiv
A great teamwork of @najung_lee_@josh_wwu Philipp Schoch, @DuncanBrownsey@JozefKristek1 and Matt Wodrich.
https://t.co/e1N3fWHEdf