Faculty of Org Chem. Trained at IIT Madras;@ U. Connecticut; @U. Pittsburgh; @U.Oxford #NewReactions, #StrainedOrg-Molecules, #Heterocycles.
Personal account
Our recent work on the synthesis of diverse azetidines via strain-release of azabicyclo[1.1.0]butanes driven by the activation with aza-o-quinone methide (aza-o-QM) is now published in OL.
Studies on the activation of azabicyclo[1.1.0]butanes by aza-ortho-quinone methides for accessing diverse azetidine derivatives by @jdsaha2000 and co-workers in #OrgLett https://t.co/0GTsSQH4dH
Nice synthesis of highly substituted pyrrolidines by the @jdsaha2000 group! Radical Carbocyclization Intercepted Reductive C‐C Bond Formation Between 1,n‐Enynes or Dienes and Electron‐Poor Olefins/Alkynes - Advanced Synthesis & Catalysis https://t.co/AGj6AkhDTc
From @jdsaha2000 and colleagues: 'Thianthrenation-promoted photoinduced alkene difunctionalization and aryl allylation with Morita–Baylis–Hillman adducts'
https://t.co/yC9Gz0Hvta
Learn about 'Hydrogen bonding-promoted tunable approach for access to aza-bicyclo-[3.3.0]octanes and cyclopenta[b] pyrroles' by Sourav Pramanik, Subhadeep Hazra and Ayan Chatterjee @jdsaha2000
Included in 2024 Emerging Investigators Collection
https://t.co/YWuQHGBWB9
Here we show in @ChemCommun, the application of azaoxyallyl cation-like species in stereoselective synthesis of biologically relevant carbohydrates (kdo glycosides in this case). Funding from international S&T cooperation DST-RFBR, @serbonline https://t.co/V6OcGhM8Iq
Our recent study on reductive C-C bond forming reaction between olefins and electron-poor vinyl cyclopronane is disclosed in #Organic Letters @JOC_OL. Chemosective MHAT and broad scope are the salient features. Funding from @serbonline@CSIR_IND. @Biplabips@SUBHADEEPHAZR12.
Use of vinyl cyclopropane (VCP) for reductive C-C bond formation with alkenes through hydrogen atom transfer (MHAT) is reported by the Saha Group @jdsaha2000 in #OrgLett. Check it out: https://t.co/jece9tKloC
Cation-Promoted Strain-Release-Driven Access to Functionalized Azetidines from Azabicyclo[1.1.0]butanes (Jaideep Saha and co-workers) @jdsaha2000 https://t.co/j16cyjGsJq
We have recently developed a unique approach to activate and transform azabicyclo[1.1.0]butanes into 1,3-functionalized azetidines with azaoxyallyl cation, which has now been published in @angew_chem
Funding from
@serbonline and @CSIR_IND
https://t.co/xVSpgx9lER