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In Science Magazine this week, DM Lab IIT Bombay review recent progress in meta and para selective aryl functionalization methods science.sciencemag.org/content/372/65…

We are delighted to share our review Science Magazine on arene diversification through distal C−H functionalisation. Debabrata Maiti IIT Bombay Science Magazine SERB Uttam Dutta @SUDIPMA74834494 @TrishaB76564473 science.sciencemag.org/content/372/65…

Glad to share our recent contribution in @Chemcommun for the synthesis of cyclophane type molecules via macrocyclization. Congrats to Bidhan, Satabdi and Pintu. pubs.rsc.org/en/content/art…

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. chemrxiv.org/engage/chemrxi… New ligands design are ongoing to strengthen this 🆕route to biaryls!

Differentiating the reactivity of aryl (pseudo)halides based on the bond dissociation enthalpy (BDE).

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 IIT Bombay Read the full review here 🔗 rsc.li/3LU1HN7 rsc.li/3LU1HN7

You can now read the paper Nature Catalysis using the following link. Thanks to DM Lab IIT Bombay Debabrata Maiti Sudip Maiti Dineshkumar Raja and all others involved.

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 Nature Catalysis Many Congratulations to Sudip Maiti , Pintu Ghosh Dineshkumar Raja, Debabrata Maiti and others

Congrats Pintu Ghosh, Sudip Maiti on their recent J. Am. Chem. Soc. article showcasing anti-Markovnikov alkene hydrocarboxylation via CO₂ radical anion utilising a synergestic triple catalytic cycle! Special thanks to our collaborator Audisio Davide. Link ⤵️ pubs.acs.org/doi/10.1021/ja…