#arylation
December 1, 2025 at 8:39 PM
Don't forget that the lead compound for vertex came from a library developed in collaboration with the Jin Quan Yu lab at Scripps, using CH functionalization

chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/...
February 22, 2025 at 8:09 PM
Development and enantioselective synthesis of spirobiindoles via Rh-catalyzed asymmetric arylation-spirocyclization sequence

doi.org/10.1016/j.cc...
May 7, 2025 at 1:00 AM
Congrats to Kathleen, Emily, and Erika from our group for their recent report on challenging Ni-catalyzed O-arylation chemistry of pharmaceutical relevance 👍

chemistry-europe.onlinelibrary.wiley.com/doi/full/10....
Nickel‐Catalyzed O‐Arylation of N‐Protected Amino Alcohols with (Hetero)aryl Chlorides
The first effective base metal-catalyzed protocol for C−O cross-coupling of primary, secondary, and tertiary alcohol-containing N-Boc protected amino alcohols with (hetero)aryl chlorides, affording a....
chemistry-europe.onlinelibrary.wiley.com
February 20, 2025 at 1:05 AM
New publication🧪🧪🧪

We’re excited to share our latest work: Ortho Arylation of N-Aryl Amides and the Construction of Diagonal Tetraarylbenzenediamines and N-Doped Fulminenes via BBr₃-Derived Dibromoboracycles

chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/...

#OranicChemistry #Organoboron
Ortho Arylation of N‐Aryl Amides and the Construction of Diagonal Tetraarylbenzenediamines and N‐Doped Fulminenes via BBr3‐Derived Dibromoboracycles
We report the discovery of a boron-driven ortho-arylation reaction of N-aryl amides and ureas. This novel method enables directed borylation of a wide range of substrates, leading to the synthesis of...
chemistry-europe.onlinelibrary.wiley.com
December 2, 2024 at 7:56 AM
Our collaboration with the Benaglia group is effective in aqueous media, facilitating the functionalization of biomolecules. The photochemical reaction is scalable under continuous flow conditions, making it suitable for large-scale applications.
#ChemSky #photocatalysis
doi.org/10.1002/chem...
Visible‐Light Photoredox Catalytic Direct N‐(Het)Arylation of Lactams
Lactam rings can be introduced to a diverse range of arenes and heteroarenes employing our mild and efficient photoredox method. The N-(het)arylation of lactams also works in aqueous media, allowing ...
doi.org
February 27, 2025 at 11:44 AM
Salem, Doucet, and co-workers investigate the palladium-catalyzed C–H arylation of 3-(hydroxymethyl)furan! The hydroxymethyl group directs regioselective arylation at C2, while C5 remains unaffected.⚗️
#Palladium #Catalysis

👉 buff.ly/R751HsW
May 12, 2025 at 7:01 AM
Development and enantioselective synthesis of spirobiindoles via Rh-catalyzed asymmetric arylation-spirocyclization sequence
Development and enantioselective synthesis of spirobiindoles via Rh-catalyzed asymmetric arylation-spirocyclization sequence

doi.org/10.1016/j.cc...
May 7, 2025 at 6:58 AM
Don't miss Heather D. Maynard, Alexander M. Spokoyny, K. N. Houk et al's recent article #ChemSciCovers

'In silico screening of P,N-ligands facilitates optimization of Au(iii)-mediated S-arylation'

🔗 doi.org/10.1039/D4SC...

#chemsky
March 2, 2025 at 10:00 AM
We built a machine learning–guided workflow to optimize reaction conditions for photochemical nickel-catalyzed cysteine arylation; no specialized robots or fancy HTE plates needed!

Check it out @chemrxiv.org : chemrxiv.org/engage/chemr...

#MachineLearning #ReactionOptimization
October 1, 2025 at 1:10 PM
Development and enantioselective synthesis of spirobiindoles via Rh-catalyzed asymmetric arylation-spirocyclization sequence

doi.org/10.1016/j.cc...
April 29, 2025 at 2:03 AM
Please see our collaboration with Tomasz J. Idzik #WPUTS #ChemSky #photocatalysis
@chemcomm.rsc.org

Metal-free visible-light-induced cascade arylation/aza-semipinacol rearrangement of β,γ-unsaturated δ-lactams
doi.org/10.1039/d6cc...
August 31, 2026 at 10:19 AM
Congrats to Shijin, Drew, and Martin on publication of this C-H arylation with remarkable terminal selectivity! 3,5-lutidine turns out to be key! Check it out in Chem Eur J @chemistryeurope.bsky.social

chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/...
Terminal Selective Arylation of Inert Alkanes via Radical‐Organometallic Crossover
Selectivity is an essential part of organic synthesis and key to synthetic efficiency. However, selectivity is challenging to achieve in hydrocarbon molecules. Herein we report a mild and direct meth....
chemistry-europe.onlinelibrary.wiley.com
September 24, 2025 at 3:41 PM
Turns out you can do cysteine profiling without lysing the cells first!

www.nature.com/articles/s41...

Led by @bendavisgroup.bsky.social and with some very deep chemoproteomics characterisation
Biocompatible ligand balancing in transition metal coordination enables benign in-cell protein arylation - Nature Chemistry
The perceived toxicity of organometallic reagents has limited their use in living systems. Now it has been shown that balancing flexible chelation with biocompatible ligands without precluding chemica...
www.nature.com
January 7, 2026 at 10:15 AM
Catalytic production of benign bisphenols from lignin via pre-arylation method. #scisky #science #news #materialscience

www.the-innovation.org/article/doi/...
November 26, 2024 at 4:02 PM
🚀Just dropped: Our new paper on solubility-enhanced dibromodibenzophenazines is now online Asian JOC! Curious about exciting new building blocks for exotic π-conjugated systems? Check it out doi.org/10.1002/ajoc... Huge congrats to Naohiro for the amazing work! 👏 #PiSky
Synthesis of Solubility‐Enhanced 6,8‐Diarylated Dibromodibenzo[a,j]Phenazines via Pd‐Catalyzed C─H Arylation and Skeletal Rearrangement
A new class of 6,8-diaryl-substituted DBPHZs has been synthesized via regioselective Pd-catalyzed C─H arylation and oxidative skeletal rearrangement. Strategically introduced bulky aryl groups bearin...
doi.org
September 23, 2025 at 10:42 PM
🚨 #chemsky mystery of the month 🚨

I’m working on an arylation reaction and need a reliable Ph donor. Ph₄BNa works great but is super wasteful. PhBF₃K gives <30% yield, so I tested the hydrolytic PhB(OH)₂ — it works but is highly irreproducible. 🤯
Other attempts:
PhBPin: No luck.
PhB(triol)K: Nope.
November 21, 2024 at 9:14 PM
Highlighting this paper on #InternationalWomensDay written for the Special Issue "Women in emerging organic and hybrid electronic materials and interfaces". advanced.onlinelibrary.wiley.com/doi/10.1002/...
Thank you to Angela Lin and Helen Tran for the collaboration! #chemsky
Soft and Stretchable Thienopyrroledione‐Based Polymers via Direct Arylation
π-conjugated polymers (CPs) that are concurrently soft and stretchable are needed for deformable electronics. This systematic molecular weight study on promising candidates for soft CPs, poly(indacen...
advanced.onlinelibrary.wiley.com
March 9, 2025 at 1:40 AM
Best solvents so far: DMSO and MeOH.
No reaction in DCM or THF.
Bases like KF, K₂CO₃, etc., don’t seem to help.

Any ideas on how to make this reaction reproducible? Would love some input! 🔬💡
#Help #Boron #ChemMystery #Arylation
November 21, 2024 at 9:14 PM
A New Year’s Day paper reports a novel Pd(OAc)₂-catalyzed reaction to yield fused imidazo[1,2-f]phenanthridine derivatives.

CSD Entry YUFTIG reveals that the process bypassed C–H and N–H arylation.

🔗 ccdc-info.com/41Ry346

#FeaturedStructureFriday #CompChemSky
January 3, 2025 at 12:11 PM
Our collaboration w/ @markstradiotto.bsky.social and team is now out in Chem. Eur. J. (@chemistryeurope.bsky.social)!

Mark's team used DalPhos ligands for Ni-cat. C-P couplings, which we supported with DFT calculations of reductive elimination.

doi.org/10.1002/chem...

@cathweetman.bsky.social
Nickel‐Catalyzed P‐Arylation of HP(= O)(R/OR)2 Nucleophiles with (Hetero)Aryl Chlorides Enabled by DalPhos Ligation
The development of broadly useful C-P cross-couplings of (hetero)aryl chlorides and HP(O)(R/OR)2 nucleophiles by use of nickel/DalPhos-based catalysts is described, along with findings from DFT studi....
doi.org
September 16, 2025 at 8:24 AM
Wang et al. in the Han Lab at Hubei Normal University demonstrate a regioselective palladium-catalyzed C3–H arylation of triazolopyridazines using aryl thianthrenium salts, achieving moderate to excellent yields and highlighting the method's broad substrate scope and functional-group tolerance.
Organic Letters
doi.org
October 1, 2026 at 6:22 AM