Subhabrata Dutta, M.Sc.

Subhabrata Dutta
© Subhabrata Dutta
Subhabrata Dutta
PhD Student
Room 408, OC/BC I
Corrensstraße 36
48149 Münster
T: +49 251 8335314
F: +49 251 8339772
sdutta@uni-muenster.de
External Profiles:
  • Curriculum Vitae

    since 02/2021 PhD thesis in the group of Prof. F. Glorius, Westfälische Wilhelms-Universität Münster
    07/2018 - 10/2020 Master of Science (M.Sc.), M.Sc. thesis at Indian Institute of Technology (IIT), Bombay, India; Supervisor: Prof. Dr. Debabrata Maiti; Title: Transition metal-catalyzed C-H allylation reactions.
    07/2015 - 06/2018 Bachelor of Science (B.Sc.), Chemistry Hons., St. Xavier’s College, Kolkata, India  
    2015 10th+2 (AISSCE, CBSE), Kendriya Vidyalaya No-2, Kalaikunda, West Bengal, India
    2013 10th (AISSE, CBSE), Kendriya Vidyalaya No-2, Kalaikunda, West Bengal, India
  • Awards and Scholarships

     
    2020 Institute Silver Medal for academic excellence in Chemistry, IIT Bombay
    2020 Prof. Hiralal Memorial Award for overall academic excellence in Master of Science, IIT Bombay
    2020 Prof. A.B. Biswas Memorial & Shri Prakash Krishnan Award Prize for securing highest GPA in Chemistry
    2020 AIR-38 in The Graduate Aptitute Test in Engineering (GATE) (Chemistry)
    2019 Institute Academic Award of Year 2018 for excellence in First year of Masters, IIT Bombay
    2019 AIR-15 in Junior Research Fellowship (JRF) CSIR-NET (Chemistry)
    2019 Qualified Junior Research Fellowship under Council for Scientific and Industrial Research (CSIR)
    2018 AIR-29 in IIT-JOINT ADMISSION TEST (Chemistry) amongst 12473 candidates
    2015 - 2019 Recipient of INSPIRE-SHE Scholarship by Government of India for being in top 1% in CBSE
    2015 CBSE Merit Cum Scholarship for securing overall 95% in AISSCE
    2013 CBSE Merit Cum Scholarship for securing CGPA 10.0 in AISCE
  • Publications

    R. Laskar,§ S. Dutta,§ J. C. Spies, P. Mukherjee, A. Renteria-Gomez, R. E. Thielemann, C. G. Daniliuc, O. Gutierrez,* F. Glorius,*
    γ-Amino Alcohols via Energy Transfer Enabled Brook Rearrangement,
    J. Am. Chem. Soc. 2024, 146, 10899-10907.
    § These authors contributed equally.

    S. Dutta, Y.-L. Lu,§ J. E. Erchinger,§ H. Shao, E. Studer, F. Schäfer, H. Wang, D. Rana, C. G. Daniliuc, K. N. Houk,* F. Glorius,*
    Double Strain-Release [2π+2σ]-Photocycloaddition,
    J. Am. Chem. Soc. 2024, 146, 5232-5241.
    § These authors contributed equally.

    S. Dutta,§ D. Lee,§ K. Ozols,§ C. Daniliuc, R. Shintani, F. Glorius,
    Photoredox-Enabled Dearomative [2π+2σ] Cycloaddition of Phenols,
    J. Am. Chem. Soc. 2024, 146, 2789-2797.

    § These authors contributed equally.

    F.-P. Wu, C. C. Chintawar, R. Lalisse, P. Mukherjee, S. Dutta, J. Tyler, C. G. Daniliuc, O. Gutierrez,* F. Glorius,*
    Ring expansion of indene by photoredox-enabled functionalized carbon-atom insertion,
    Nat. Catal. 2024, asap. DOI

    S. Dutta, J. E. Erchinger, F. Strieth-Kalthoff, R. Kleinmans, F. Glorius,
    Energy transfer photocatalysis: exciting modes of reactivity,
    Chem. Soc. Rev. 2024, 53, 1068-1089.

    T. Bhattacharya, S. Ghosh, S. Dutta, S. Guin, A. Ghosh, H. Ge,* R. B. Sunoj,* D. Maiti,*
    Combinatorial Ligand Assisted Simultaneous Control of Axial and Central Chirality in Highly Stereoselective C−H Allylation,
    Angew. Chem. Int. Ed. 2023, 62, e202310112, Early View.  DOI

    H. Wang,§ J. E. Erchinger,§ M. Lenz,§ S. Dutta, C. G. Daniliuc, F. Glorius,
    syn-Selective Difunctionalization of Bicyclobutanes Enabled by Photoredox-Mediated C–S σ-Bond Scission,
    J. Am. Chem. Soc. 2023, 145, 23771-23780.
    § These authors contributed equally

    H. Wang, H. Shao,§ A. Das,§ S. Dutta, H. T. Chan, C. Daniliuc, K. N. Houk,* F. Glorius,*
    Dearomative ring expansion of thiophenes by bicyclobutane insertion,
    Science 2023, 381, 75-81.
    § These authors contributed equally

    Free-access electronic reprint

    R. Kleinmans,§ S. Dutta,§ K. Ozols, H. Shao, F. Schäfer, R. E. Thielemann, H. T. Chan, C. G. Daniliuc, K. N. Houk,* F. Glorius,*
    ortho-Selective Dearomative [2π + 2σ]-Photocycloadditions of Bicyclic Aza-Arenes,
    J. Am. Chem. Soc. 2023, 145, 12324-12332.
    § These authors contributed equally

    A. Kaithal, H. Sekhar Sasmal, S. Dutta, F. Schäfer, L. Schlichter, F. Glorius,
    cis-Selective Hydrogenation of Aryl Germanes: A Direct Approach to Access Saturated Carbo- and Heterocyclic Germanes,
    J. Am. Chem. Soc. 2023, 145, 4109-4118.

    J. E. Erchinger, R. Hoogesteger,§ R. Laskar,§ S. Dutta, C. Hümpel, D. Rana, C. G. Daniliuc, F. Glorius,
    EnT-Mediated N–S Bond Homolysis of a Bifunctional Reagent Leading to Aliphatic Sulfonyl Fluorides,
    J. Am. Chem. Soc. 2023, 145, 2364-2374.
    § These authors contributed equally

    S. Dutta,§ J. E. Erchinger,§ F. Schäfers, A. Das, C. G Daniliuc, F. Glorius,
    Chromium/Photoredox Dual-Catalyzed Synthesis of α-Benzylic Alcohols, Isochromanones, 1,2-Oxy Alcohols and 1,2-Thio Alcohols,
    Angew. Chem. Int. Ed. 2022, 61, e202212136.
    § These authors contributed equally

    F. Schäfers,§ S. Dutta,§ R. Kleinmans, C. Mück-Lichtenfeld, F. Glorius,
    Asymmetric Addition of Allylsilanes to Aldehydes – A Cr/Photoredox Dual Catalytic Approach Complementing the Hosomi–Sakurai Reaction,
    ACS Catal. 2022, 12, 12281-12290.
    § These authors contributed equally
     

    S. Dutta, S. Chatterjee, S. A. Al-Thabaiti, S. Bawaked, M. Mokhtar, D. Maiti,
    C–H activation: A strategic approach toward lactams using transition metals,
    ChemCatalysis 2022, 2, 1046-1083.

    R. Kleinmans,§ T. Pinkert,§ S. Dutta, T. O. Paulisch, H. Keum, C. G. Daniliuc, F. Glorius,
    Intermolecular [2π+2σ]-photocycloaddition enabled by triplet energy transfer,
    Nature 2022, 605, 477-482.

    § These authors contributed equally

    L. Quach, S. Dutta, P. M. Pflüger, F. Sandfort, P. Bellotti, F. Glorius,
    Visible-Light-Initiated Hydrooxygenation of Unactivated Alkenes - A Strategy for Anti-Markovnikov Hydrofunctionalization,
    ACS Catal. 2022, 12, 2499-2504.

    S. R. Sahoo, S. Dutta, S. A. Al-Thabaiti, M. Mokhtar, D. Maiti,
    Transition metal catalyzed C–H bond activation by exo-metallacycle intermediates,
    Chem. Commun. 2021, 57, 11885-11903.

    T. Bhattacharya, S. Dutta, D. Maiti,
    Deciphering the Role of Silver in Palladium-Catalyzed C–H Functionalizations,
    ACS Catal. 2021, 11, 9702-9714.

    S. Basak, S. Dutta, D. Maiti,
    Accessing C2-Functionalized 1,3-(Benz)azoles through Transition Metal-Catalyzed C−H Activation,
    Chem. Eur. J. 2021, 27, 10533-10557.

    S. Dutta, T. Bhattacharya, D. B. Werz, D. Maiti,
    Transition Metal-Catalyzed C-H Allylation Reactions,
    Chem. 2021, 7, 1-51.

    A. Baccalini, S. Vergura, P. Dolui, S. Maiti, S. Dutta, S. Maity, F. F. Khan, G. K. Lahiri, G. Zanoni, D. Maiti,
    Cobalt-Catalysed C(sp2)-H Allylation of Biphenyl Amines with Unbiased Terminal Olefin,
    Org. Lett. 2019, 21, 8842-8846.

  • Research Experiences

     
    06/2019 - 05/2020 Transient Directing Group (DG ) Assited Atroposelective Allylation Of Axially Chiral Biaryls; Guide: Dr. Debabrata Maiti, IIT Bombay, Mumbai
    04/2019 - 06/2019 Cobalt-Catalyzed C(sp2)-H Allylation of Biphenyl Amines with Unbiased Terminal Olefins; Guide: Dr. Debabrata Maiti, IIT Bombay, Mumbai
    08/2017 - 03/2018 DNA: A Nano-Scale ApproachTowards Delineation Of Its Structure (review thesis); Guide: Dr. Indranil Chakraborty, St.Xavier’s College, Kolkata
  • Professional Experience & Training

     
    2018 - 2020 Subject Matter Expert in CHEGG PRIVATE LIMITED
      Member of Institute Student Companion Programme (ISCP)
    05/2018 - 06/2018 intern in FRANBIZ CORP
      Tutor in TOPPR COMMUNITY
    2018 Seminar Hall manager for NATIONAL SYMPOSIUM ON FACETS OF CHEMISTRY IN MATERIAL & BIOLOGY
    (FOCMB-I), Department of Chemistry, St.Xavier’s College, Kolkata
    2017 Student coordinator in INTERNATIONAL SYMPOSIUM ON FACETS OF CHEMISTRY IN BIOLOGY
    (FOCB-II), Department of Chemistry, St.Xavier’s College, Kolkata
  • Skills & Activities

    •    Volunteer in National Service Scheme (NSS)

    •    5 Year Senior Diploma in painting

    •    Distinction grade in painting & theory