Congrats @PintuGh90578115, @smaitichem on their recent @J_A_C_S article showcasing anti-Markovnikov alkene hydrocarboxylation via CO₂ radical anion utilising a synergestic triple catalytic cycle!
Special thanks to our collaborator @DavideAudisio.
Link ⤵️
https://t.co/IRPSKjBdjI
Want to gain the cross selectivity in C(sp2)-C(sp2) XEC?
Now we could stitch two aryl halides avoiding the traditional transmetalation step.
Check out @NatureCatalysis
Many Congratulations to @smaitichem , @PintuGh90578115 @Dinesh_Rajaa, @maiti_iitb and others
♨️off the Press @NatureCatalysis, @dm_lab@serbonline.
Now you can cross-couple two aryl halides by single metal.
This new method of cross-electrophile coupling exploited both the excited & ground state chemistry of palladium bypassing transmetalation.
https://t.co/9WxLWyk1YL
Out now as part of our #PioneeringInvestigators collection
"Transition-metal catalyzed C–H activation as a means of synthesizing complex natural products" by Debabrata Maiti & co.
@dm_lab
Read the full review here 🔗
https://t.co/6bLitQ6qr5
https://t.co/6bLitQ6qr5
Excited Pd-catalyst performs the magic trick for the cross-electrophile coupling! Rational ligand design helps to improve the selectivity of a cross-coupled product. Now on @ChemRxiv.
https://t.co/sc5eqh1TEt
New ligands design are ongoing to strengthen this 🆕route to biaryls!
Glad to share our recent contribution in @Chemcommun for the synthesis of cyclophane type molecules via macrocyclization. Congrats to Bidhan, Satabdi and Pintu.
https://t.co/6DWfIUPVNc