Anirudh Dixit

[The Dong Lab @GBD_Lab]

Our recent work on aliphatic CO-to-N atom swap enabled by NAHA chemistry, now online in @ScienceMagazine ! Congratulations to Zining, Zhehan and @RongYehhh !
https://t.co/wvtKrbLgYY

[AggarwalLab @AggarwalLab]

Our latest work with @duarte_group shows the unexpected exo-C2 lithiation of ABP and ABH, allowing access to ring-opening products with full stereocontrol.

Congrats Team!

#OrganicChemistry #StrainRelease @BristolChem

https://t.co/ifzhserezI

[Ryoma Shimazumi @ryoma_ous]

Photoinduced Disproportionation Enables Oxidative Addition of Aryl Iodides at a Gallium(I) Center | ChemRxiv
👏 https://t.co/8Xff3vi8Dk

[Anirudh Dixit @Rud01N]

@buddhadeb1979 @mirjahassan @saikat_orgchm @anogh_ghosh @PriyonuM84736 @ChattopadhyayL1 @IISERPune @ChemicalScience @sunojchemlab @iitbombay @ANRFIndia nice chemistry. but just a question can we really isolate this intermediate species that is proposed in article. congratulations again to the team.

[Buddhadeb Chattopadhyay @buddhadeb1979]

Congratulations @mirjahassan, @saikat_orgchm, @anogh_ghosh, @PriyonuM84736 from @ChattopadhyayL1 group @IISERPune for @ChemicalScience! An excellent collaboration with @sunojchemlab @iitbombay! An unprecedented “boron-walking-mechanism. Thanks @ANRFIndia.
https://t.co/QqD5wwztay

[Boron-Chem-Research @Boron_Chemistry]

Direct Access to Carbenoids from Alkyl and α-Acyloxy Halides for Boron Homologations ( @ChemRxiv ): https://t.co/Fo8D31esw8 ( @AThomasLab ).

[Honggen Wang @Honggen_W]

Our new publication exploring β-Boron in metal catalysis : β-Boron or β-Silicon Effect Enables a Regioselective Ni-Catalyzed Hydrocyanation of Internal Alkynes - now published in Green Chemistry https://t.co/E1dF49Unlo

[Gabriele Laudadio @g_laudadio]

Another great work from @ParasramLab !

Nitro groups do not look so scary anymore :)

https://t.co/eqyaLdiV2s

[Princeton Chemistry @PrincetonChem]

The David MacMillan Lab @macmillan_lab advances a couple-close strategy to make “the impossible, possible.” Great work Jiaxin (Jay), Will, Johnny, Will, Noriyuki, Alice, Taylor, Chris, Marian, Dave!

Enjoy our story on the lab’s new research in Science: https://t.co/aHbaGFgCBD

[The Hartwig Group @HartwigGroup]

Our postdoc @Willi_Amberg built @SynStrategy a learning tool that categorizes 500+ reactions by functional group with 400+ total synthesis examples. If you’re into #OrgChem, check it out (it’s free)!

iOS: https://t.co/vTpNTwl4ZU
Android: https://t.co/yMQsiJUZU6

#ChemTwitter

[Yuki Nagashima @YukiNagash]

Our latest paper has been published in Angew. Chem. Int. Ed. @angew_chem !
“Photoinduced Generation of (Boryl)Silyl and (Chloro)Silyl Radicals: Access to Trisubstituted Silylboranes and Chlorosilanes ”
https://t.co/RFxreNRdMR

[Narayan Lab @ UMich @NarayanLab]

Check out our synthesis of enantioenriched atropisomers in Nature!
https://t.co/TtH0VzfEMv

[The Parasram Lab @ParasramLab]

Check out our recent collaborative work published in @Chem_CP with the @VetticattGroup on the first example of using photoexcited nitroarenes for PCET-enabled decarboxylative oxygenation of acids. @nyuniversity @nyuchemistry #PCET #synthesis #photochem https://t.co/N3yP00fP8S

[The Maji Research Group @MajiGroupIISERK]

On DCS-Day, we premiered our Lab video 🎥🧪- a snapshot of our people, passion, and the science we love. From ideas to experiments, it’s a glimpse into the energy and chemistry that power our lab! ✨🔥
@bm_iiserk @dcsiiserkol @iiserkol

[Chemistry News @ChemistryNews]

A new three-way single step rearrangement enables precise ring editing https://t.co/c8ucFKnZPL

[Jiawei Sun @Jiawei1024]

Another breakthrough!! A “Nose Ring” for a wild radical has been installed using a sulfonyl hydrazide. The Ni–diazene intermediate guides the radical to find the right partner (alkyl iodide), enabling precise control of stereochemistry. Please check out our latest RRCC reaction!!

[Spirocycles @spirocycles]

🔬 50 g flow-scalable Spiro-Piperidine synthesis!

A photoredox/HAT dual catalytic annulation converts unprotected primary amines into δ-lactams-gateways to α-disubstituted & spirocyclic piperidines.
Mild condition and highly diversifiable-opening new space for drug discovery 🚀from @UniofBath in collab with @EnamineLtd & @SyngentaUK
🔗https://t.co/2tfdKTp2mr

[Jacsol Joc @jacsoljoc]

https://t.co/pi5I52726W

[The Hari Group @HariGroupIISc]

🚀Ring-expansion of ketones with [1.1.1]propellane to access functionalized MCB-ketones and spirocyclic scaffolds is out @J_A_C_S. A great collaboration with @MykhailiukChem. Thank you, @ANRFIndia and @iiscbangalore, for the financial support. https://t.co/kSouq7umuH

[The Maji Research Group @MajiGroupIISERK]

🎉Our lab alumnus Dr. Satyadeep Waiba @SatyadeepW has joined the Department of Chemistry, @IITBombay, as an Assistant Professor! 👏
We’re incredibly proud of his achievement and wish him continued success in this exciting new chapter! 🔬✨
@bm_iiserk @dcsiiserkol
#ProudMoment