chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/...
chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/...
doi.org/10.1016/j.cc...
doi.org/10.1016/j.cc...
chemistry-europe.onlinelibrary.wiley.com/doi/full/10....
chemistry-europe.onlinelibrary.wiley.com/doi/full/10....
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
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
#ChemSky #photocatalysis
doi.org/10.1002/chem...
#ChemSky #photocatalysis
doi.org/10.1002/chem...
#Palladium #Catalysis
👉 buff.ly/R751HsW
#Palladium #Catalysis
👉 buff.ly/R751HsW
doi.org/10.1016/j.cc...
'In silico screening of P,N-ligands facilitates optimization of Au(iii)-mediated S-arylation'
🔗 doi.org/10.1039/D4SC...
#chemsky
'In silico screening of P,N-ligands facilitates optimization of Au(iii)-mediated S-arylation'
🔗 doi.org/10.1039/D4SC...
#chemsky
Check it out @chemrxiv.org : chemrxiv.org/engage/chemr...
#MachineLearning #ReactionOptimization
Check it out @chemrxiv.org : chemrxiv.org/engage/chemr...
#MachineLearning #ReactionOptimization
doi.org/10.1016/j.cc...
doi.org/10.1016/j.cc...
@chemcomm.rsc.org
Metal-free visible-light-induced cascade arylation/aza-semipinacol rearrangement of β,γ-unsaturated δ-lactams
doi.org/10.1039/d6cc...
@chemcomm.rsc.org
Metal-free visible-light-induced cascade arylation/aza-semipinacol rearrangement of β,γ-unsaturated δ-lactams
doi.org/10.1039/d6cc...
chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/...
chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/...
www.nature.com/articles/s41...
Led by @bendavisgroup.bsky.social and with some very deep chemoproteomics characterisation
www.nature.com/articles/s41...
Led by @bendavisgroup.bsky.social and with some very deep chemoproteomics characterisation
www.the-innovation.org/article/doi/...
www.the-innovation.org/article/doi/...
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.
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.
Thank you to Angela Lin and Helen Tran for the collaboration! #chemsky
Thank you to Angela Lin and Helen Tran for the collaboration! #chemsky
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
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
CSD Entry YUFTIG reveals that the process bypassed C–H and N–H arylation.
🔗 ccdc-info.com/41Ry346
#FeaturedStructureFriday #CompChemSky
CSD Entry YUFTIG reveals that the process bypassed C–H and N–H arylation.
🔗 ccdc-info.com/41Ry346
#FeaturedStructureFriday #CompChemSky
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
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