BS Research Group IISER TVM
@TheSahooGroup
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Organic Synthesis & Catalysis Laboratory @chemie_iisertvm @tvmiiser
Thiruvananthapuram
Joined December 2022
🎓 PhD Opportunity @TheSahooGroup
@tvmiiser Join cutting-edge research in catalysis for Sustainable Organic Synthesis 🧪 Eligible: UGC/CSIR-JRF holders 🔗 Portal: https://t.co/fDyuTPbcsB
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Happy to share that our work on azidation and cyanation has been featured on Organic Chemistry Portal ( https://t.co/9hLZexUviB). Grateful for the recognition. Feel free to have a look!!! @153Basu @sandipyquimica @itsAD09
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Kudos to @Subham_3005, @SnehajitChakra3 and co. for their efforts.
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A simple reductant-controlled approach to Sulfinamides from Amines via formal SO insertion to C-N bond — now published in @JOC_OL (@ACSPublications )! 🔬 Thanks to @CSIR_IND for the financial support !!! @Chemie_iisertvm @tvmiiser
https://t.co/An7t3IVj3V
pubs.acs.org
The conversion of primary amines into sulfinamides through formal sulfoxide (SO) insertion into stronger C–N bonds offers a challenging yet compelling approach for subtle functional group editing, in...
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Our group member Amit Pal @Photochem_Amit presented his work on “Heavier Dihydropyridine (DHP) Chalcogenol Esters in Hydrothio(seleno)carbonylation Enabled by Metallaphotoredox Catalysis” at the XX J-NOST @NOST_India Conference held at @IITISM_DHANBAD
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We are pleased to announce that Prof. Basudev Sahoo (IISERThiruvananthapuram) will deliver an invited lecture at OCS–ECR 2026. 📍 Venue: Indian Institute of Technology Jodhpur, India 🗓️ Dates: 27–28 February 2026 🌐 Website: https://t.co/Dsc6zNNQ4I
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We are delighted to welcome Prof. Basudev Sahoo from IISER Thiruvananthapuram @153Basu ( https://t.co/NBjbc3IdLJ ), as an Invited Speaker in @ChemSpirit2025, at IIT Hyderabad.
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🚨 We are thrilled to share that our group member, @Photochem_Amit, attended @omcos22 at Kyoto University, Japan 🇯🇵! He presented his poster titled "Heavier Dihydropyridine (DHP) Chalcogenol Esters in Hydrothio(seleno)carbonylation Enabled by Metallaphotoredox Catalysis."
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Huge congratulations to the BS Group grads🎓!! You made it !!!! Time to chase your dreams and make a mark. All the very best for your upcoming adventure! 🚀
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Thrilled to announce our group's latest research published in @J_A_C_S! Huge congratulations to Kaushalendra Patel @kaushalendrapat, Leonie Wilczek, and Francesco Calogero @fncclg for this outstanding contribution. Well done, all! 🥳👏@ACSPublications
https://t.co/e5msXqt4FU
pubs.acs.org
We present a stereoretentive nucleophilic substitution of homoallylic tertiary alcohols via the formation of a nonclassical cyclopropyl carbinyl (CPC) carbocation intermediate. This strategy enables...
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Hot Off the Press!!🚨 Excited to share our lab's first publication in @angew_chem. "PCET Photodecarboxylation for SN2’-Type Alkylation of gem- Dichlorocyclobutenones" is now online! @MoE and @tvmiiser @Chemie_iisertvm support and funding. https://t.co/vyjFYC1qFN
onlinelibrary.wiley.com
A versatile radical SN2’-type alkylation of gem-dichlorocyclobutenones is reported by photodecarboxylation of free carboxylic acids via proton-coupled electron transfer (PCET). This mild and scalab...
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Hot Off the Press!!🚨 Excited to share our lab's first publication in @angew_chem. "PCET Photodecarboxylation for SN2’-Type Alkylation of gem- Dichlorocyclobutenones" is now online! @MoE and @tvmiiser @Chemie_iisertvm support and funding. https://t.co/vyjFYC1qFN
onlinelibrary.wiley.com
A versatile radical SN2’-type alkylation of gem-dichlorocyclobutenones is reported by photodecarboxylation of free carboxylic acids via proton-coupled electron transfer (PCET). This mild and scalab...
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DHP thioester shines again in Organic Letters!! We showed here a branch-selective thiocarbonylation of alkenes via metallophotoredox catalysis. Hard work paid off by @Photochem_Amit, @sandipyquimica @sariga, thanks to @serbonline for financial support .
pubs.acs.org
We describe for the first time a photochemical branched hydrothiocarbonylation of vinyl arenes with bench-stable 1,4-dihydropyridine thioesters to furnish various thioesters in high regioselectivity....
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DHP thioester shines again in Organic Letters!! We showed here a branch-selective thiocarbonylation of alkenes via metallophotoredox catalysis. Hard work paid off by @Photochem_Amit, @sandipyquimica @sariga, thanks to @serbonline for financial support .
pubs.acs.org
We describe for the first time a photochemical branched hydrothiocarbonylation of vinyl arenes with bench-stable 1,4-dihydropyridine thioesters to furnish various thioesters in high regioselectivity....
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Explore our latest highlights on "Cu-Nanoclusters as Emerging Catalysts in Organic Synthesis," featured in @synlett_journal. We extend our gratitude to Prof. Negishi and Dr. Sourav Biswas for their collaboration.@153Basu @Chemie_iisertvm @Photochem_Amit @exceptionIN
Explore the evolving world of Cu #nanoclusters!🔬Sahoo (@153Basu), Negishi & co-workers highlight how precise synthesis, ligand selection, and structural tuning enhance stability and catalytic performance🚀 #Nanotechnology #Catalysis Read more👉 https://t.co/TTVzzd9cU0
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Please check out our research on #Skeletal Editing of N-heterocycles using Sulfenylcarbenes published in the Journal of the American Chemical Society (@J_A_C_S ).
pubs.acs.org
Late-stage functionalization (LSF) is a crucial strategy in drug discovery, allowing the modification of complex molecules, including pharmaceuticals, to enhance chemical diversity in drug libraries....
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In case you missed it, from @TheSahooGroup, @Photochem_Amit and co. 'Photocatalytic C–C bond thio(seleno)esterification of 1,2-diketone-derived pro-aromatic intermediates' #OpenAccess 🔓 @chemie_iisertvm, @tvmiiser, @153Basu
https://t.co/kUhmqagS1b
pubs.rsc.org
We report an organophotocatalyst-enabled oxidant-free C–S/C–Se bond coupling of (un)symmetrical 1,2-diketones via pro-aromatic dihydroquinazolinones/benzothiazolines, employing readily accessible...
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Breaking News from IISER TVM! PhD advertisement for Varsha 2025 Admissions is published on our website. The online application portal will be open from 1st April 2025. https://t.co/70ZIjq9L0T
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