Modhu Sudan Maji, PhD - Publications

Affiliations: 
2013- Chemistry Indian Institute of Technology Kharagpur, Kharagpur, West Bengal, India 
Area:
Heterocycle Chemistry, Alkaloids Total Synthesis, C-H Bond Functionalization, PAH
Website:
https://www.msmlabiitkgp.com/msm

54 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Das S, Kundu S, Metya A, Maji MS. A toolbox approach to revealing a series of naphthocarbazoles to showcase photocatalytic reductive syntheses. Chemical Science. 15: 13466-13474. PMID 39183925 DOI: 10.1039/d4sc03438d  0.815
2024 Bhunia S, Karan G, Snehil S, Maji MS. Direct Asymmetric Synthesis of α-Aminoimines from 1,2-Bis-N-Sulfinylimines by Using Allyl Boronic Acids. Angewandte Chemie (International Ed. in English). e202408886. PMID 39078686 DOI: 10.1002/anie.202408886  0.83
2024 Kundu S, Roy L, Maji MS. Correction to "Development of Carbazole-Cored Organo-Photocatalyst for Visible Light-Driven Reductive Pinacol/Imino-Pinacol Coupling". Organic Letters. PMID 38804695 DOI: 10.1021/acs.orglett.3c03217  0.673
2024 Karan G, Sahu S, Metya A, Maji MS. Asymmetric 1,2-Migration on Vicinal Tetrasubstituted Stereocenters Constructed from α-Keto Imines. Angewandte Chemie (International Ed. in English). e202405212. PMID 38721919 DOI: 10.1002/anie.202405212  0.811
2024 Kundu S, Ghosh C, Metya A, Banerjee A, Maji MS. Carbazoquinocin Analogues as Small Molecule Biomimetic Organocatalysts in Dehydrogenative Coupling of Amines. Organic Letters. 26: 1705-1710. PMID 38373273 DOI: 10.1021/acs.orglett.4c00229  0.794
2024 Kundu S, Maji MS. Solution-Phase Late-Stage Chemoselective Photocatalytic Removal of Sulfonyl and Phenacyl Groups in Peptides. Chemistry (Weinheim An Der Bergstrasse, Germany). e202400033. PMID 38345998 DOI: 10.1002/chem.202400033  0.69
2023 Ghosh M, Sahu S, Saha S, Maji MS. Construction of C2-indolyl-quaternary centers by branch-selective allylation: enabling concise total synthesis of the (±)-mersicarpine alkaloid. Chemical Science. 15: 1789-1795. PMID 38303951 DOI: 10.1039/d3sc04732f  0.796
2023 Bhattacharyya A, Sk MR, Sen S, Kundu S, Maji MS. Annulative π-Extension by Cp*Co(III)-Catalyzed Ketone-Directed -Annulation: An Approach to Access Fused Arenes. Organic Letters. PMID 38032281 DOI: 10.1021/acs.orglett.3c03443  0.82
2023 Sk MR, Bhattacharyya A, Saha S, Brahma A, Maji MS. Annulative π-Extension by Rh(III)-Catalyzed Ketone-Directed C-H Activation: Rapid Access to Pyrenes and Related PAHs. Angewandte Chemie (International Ed. in English). e202305258. PMID 37218605 DOI: 10.1002/anie.202305258  0.833
2022 Kundu S, Roy L, Maji MS. Development of Carbazole-Cored Organo-Photocatalyst for Visible Light-Driven Reductive Pinacol/Imino-Pinacol Coupling. Organic Letters. PMID 36469513 DOI: 10.1021/acs.orglett.2c03600  0.707
2022 Saha S, Maji MS. Cp*Co(III)-catalyzed thiocarbamate-directed C-H aminocarbonylation, amination, and cascade annulation of pyrroles. Chemical Communications (Cambridge, England). 58: 10865-10868. PMID 36074776 DOI: 10.1039/d2cc03992c  0.644
2022 Sahu S, Banerjee A, Kundu S, Bhattacharyya A, Maji MS. Synthesis of functionalized indoles cascade benzannulation strategies: a decade's overview. Organic & Biomolecular Chemistry. 20: 3029-3042. PMID 35332905 DOI: 10.1039/d2ob00187j  0.779
2022 Sahu S, Karan G, Roy L, Maji MS. An expeditious route to sterically encumbered nonproteinogenic α-amino acid precursors using allylboronic acids. Chemical Science. 13: 2355-2362. PMID 35310508 DOI: 10.1039/d1sc06259j  0.8
2022 Banerjee A, Saha S, Maji MS. Cascade Benzannulation Approach for the Syntheses of Lipocarbazoles, Carbazomycins, and Related Alkaloids. The Journal of Organic Chemistry. 87: 4343-4359. PMID 35253429 DOI: 10.1021/acs.joc.2c00042  0.829
2021 Kundu S, Banerjee A, Pal SC, Ghosh M, Maji MS. Cascade annulative π-extension for the rapid construction of carbazole based polyaromatic hydrocarbons. Chemical Communications (Cambridge, England). PMID 34008629 DOI: 10.1039/d1cc00668a  0.813
2021 Karan G, Sahu S, Maji MS. A one-pot "back-to-front" approach for the synthesis of benzene ring substituted indoles using allylboronic acids. Chemical Communications (Cambridge, England). PMID 33908966 DOI: 10.1039/d1cc01512e  0.826
2020 Mondal H, Sk MR, Maji MS. Cooperativity within the catalyst: alkoxyamide as a catalyst for bromocyclization and bromination of (hetero)aromatics. Chemical Communications (Cambridge, England). PMID 32857067 DOI: 10.1039/D0Cc04673F  0.762
2020 Bera SS, Maji MS. Carbamates: A Directing Group for Selective C-H Amidation and Alkylation under Cp*Co(III) Catalysis. Organic Letters. 22: 2615-2620. PMID 32207626 DOI: 10.1021/Acs.Orglett.0C00589  0.824
2020 Saha S, Maji MS. One-pot access to tetrahydrobenzo[c]carbazoles from simple ketones by using O as an oxidant. Organic & Biomolecular Chemistry. PMID 32068756 DOI: 10.1039/C9Ob02751C  0.673
2020 Sk MR, Maji MS. Cobalt(iii)-catalyzed ketone-directed C–H vinylation using vinyl acetate Organic Chemistry Frontiers. 7: 19-24. DOI: 10.1039/C9Qo01164A  0.45
2020 Biswas A, Mondal H, Maji MS. Synthesis of Heterocycles by Isothiourea Organocatalysis Journal of Heterocyclic Chemistry. DOI: 10.1002/Jhet.4119  0.787
2020 Sk R, Bera SS, Basuli S, Metya A, Maji MS. Recent Progress in the C–N Bond Formation via High‐Valent Group 9 Cp*M(III)‐Catalyzed Directed sp2C–H Activation Asian Journal of Organic Chemistry. DOI: 10.1002/Ajoc.202000367  0.73
2019 Kundu S, Banerjee A, Maji MS. A Brønsted Acid Catalyzed Tandem Pinacol-Type Rearrangement for the Synthesis of α-(3-Indolyl) Ketones by Using α-Hydroxy Aldehydes. The Journal of Organic Chemistry. PMID 31747752 DOI: 10.1021/Acs.Joc.9B02474  0.826
2019 Banerjee A, Maji MS. A Brønsted Acid Catalyzed Cascade Reaction for the Conversion of Indoles into α-(3-Indolyl) Ketones Using 2-Benzyloxy Aldehydes. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31283058 DOI: 10.1002/Chem.201902268  0.814
2019 Debbarma S, Sk MR, Modak B, Maji MS. On-Water Cp*Ir(III)-Catalyzed C-H Functionalization for the Synthesis of Chromones through Annulation of Salicylaldehydes with Diazo-Ketones. The Journal of Organic Chemistry. PMID 31002245 DOI: 10.1021/Acs.Joc.9B00418  0.779
2019 Debbarma S, Bera SS, Maji MS. Harnessing Stereospecific Z-Enamides through Silver-Free Cp*Rh(III) Catalysis by Using Isoxazoles as Masked Electrophiles. Organic Letters. PMID 30653323 DOI: 10.1021/Acs.Orglett.8B04130  0.811
2018 Banerjee A, Guin A, Saha S, Mondal A, Maji MS. Formal [4 + 2] benzannulation of 2-alkenyl indoles with aldehydes: a route to structurally diverse carbazoles and bis-carbazoles. Organic & Biomolecular Chemistry. PMID 30566164 DOI: 10.1039/C8Ob02875C  0.83
2018 Bera SS, Sk MR, Maji MS. Weakly Coordinating Ketone-Directed Cp*Co(III)- and Cp*Rh(III)-Catalyzed C-H Amidation of Arenes: A Route to Acridone Alkaloids. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30475423 DOI: 10.1002/Chem.201805376  0.852
2018 Saha S, Banerjee A, Maji MS. Brønsted Acid Catalyzed One-Pot Benzannulation of 2-Alkenylindoles under Aerial Oxidation: A Route to Carbazoles and Indolo[2,3- a]carbazole Alkaloids. Organic Letters. PMID 30358409 DOI: 10.1021/Acs.Orglett.8B03063  0.826
2018 Sahu S, Das B, Maji MS. Stereodivergent Total Synthesis of Hapalindoles, Fischerindoles, Hapalonamide H, and Ambiguine H Alkaloids by Developing a Biomimetic, Redox-Neutral, Cascade Prins-Type Cyclization. Organic Letters. 20: 6485-6489. PMID 30336678 DOI: 10.1021/Acs.Orglett.8B02804  0.822
2018 Sk MR, Bera SS, Maji MS. Weakly Coordinating, Ketone-Directed Cp*Co(III)-Catalyzed C-H Allylation on Arenes and Indoles. Organic Letters. 20: 134-137. PMID 29256613 DOI: 10.1021/Acs.Orglett.7B03440  0.849
2018 Sk MR, Bera SS, Maji MS. Cp*Co(III)‐Catalyzed C−H Alkenylation of Aromatic Ketones with Alkenes Advanced Synthesis & Catalysis. 361: 585-590. DOI: 10.1002/Adsc.201801385  0.817
2018 Bera SS, Debbarma S, Jana S, Maji MS. Cover Picture: Cobalt(III)-Catalyzed Construction of Benzofurans, Benzofuranones and One-Pot Orthogonal C−H Functionalizations to Access Polysubstituted Benzofurans (Adv. Synth. Catal. 11/2018) Advanced Synthesis & Catalysis. 360: 2062-2062. DOI: 10.1002/Adsc.201800646  0.805
2018 Bera SS, Debbarma S, Jana S, Maji MS. Cobalt(III)-Catalyzed Construction of Benzofurans, Benzofuranones and One-Pot Orthogonal C−H Functionalizations to Access Polysubstituted Benzofurans Advanced Synthesis & Catalysis. 360: 2204-2210. DOI: 10.1002/Adsc.201800298  0.805
2017 Chakrabarti K, Maji M, Panja D, Paul B, Shee S, Das GK, Kundu S. Utilization of MeOH as a C1 Building Block in Tandem Three-Component Coupling Reaction. Organic Letters. PMID 28840733 DOI: 10.1021/Acs.Orglett.7B02105  0.325
2017 Wübbolt S, Maji MS, Irran E, Oestreich M. A Tethered Ru-S Complex with an Axial Chiral Thiolate Ligand for Cooperative Si-H Bond Activation: Application to Enantioselective Imine Reduction. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28191742 DOI: 10.1002/Chem.201700304  0.803
2017 Sahu S, Banerjee A, Maji MS. Transition-Metal-Free Redox-Neutral One-Pot C3-Alkenylation of Indoles Using Aldehydes. Organic Letters. PMID 28080068 DOI: 10.1021/Acs.Orglett.6B03612  0.83
2017 Banerjee A, Sahu S, Maji MS. Benzannulation of 2-Alkenylindoles using Aldehydes by Sequential Triple-Relay Catalysis: A Route to Carbazoles and Carbazole Alkaloids Advanced Synthesis & Catalysis. 359: 1860-1866. DOI: 10.1002/Adsc.201700092  0.821
2016 Bera SS, Debbarma S, Ghosh AK, Chand S, Maji MS. Cp*Co(III)-Catalyzed syn-Selective C-H Hydroarylation of Alkynes Using Benzamides: An Approach Toward Highly Conjugated Organic Frameworks. The Journal of Organic Chemistry. PMID 27992200 DOI: 10.1021/Acs.Joc.6B02516  0.816
2016 Debbarma S, Bera SS, Maji MS. Cp*Rh(III)-Catalyzed Low Temperature C-H Allylation of N-Aryl-trichloro Acetimidamide. The Journal of Organic Chemistry. 81: 11716-11725. PMID 27934461 DOI: 10.1021/Acs.Joc.6B02150  0.816
2014 Hong X, Küçük HB, Maji MS, Yang YF, Rueping M, Houk KN. Mechanism and selectivity of N-triflylphosphoramide catalyzed (3(+) + 2) cycloaddition between hydrazones and alkenes. Journal of the American Chemical Society. 136: 13769-80. PMID 25226575 DOI: 10.1021/Ja506660C  0.601
2014 Parmar D, Maji MS, Rueping M. Catalytic and asymmetric fluorolactonisations of carboxylic acids through anion phase transfer. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 83-6. PMID 24356866 DOI: 10.1002/Chem.201303385  0.585
2012 Rueping M, Maji MS, Küçük HB, Atodiresei I. Asymmetric Brønsted acid catalyzed cycloadditions--efficient enantioselective synthesis of pyrazolidines, pyrazolines, and 1,3-diamines from N-acyl hyrazones and alkenes. Angewandte Chemie (International Ed. in English). 51: 12864-8. PMID 23161809 DOI: 10.1002/Anie.201205813  0.616
2012 Rueping M, Dufour J, Maji MS. Relay catalysis: combined metal catalyzed oxidation and asymmetric iminium catalysis for the synthesis of bi- and tricyclic chromenes. Chemical Communications (Cambridge, England). 48: 3406-8. PMID 22363938 DOI: 10.1039/C2Cc00129B  0.625
2012 Rueping M, Maji MS, Küçük HB, Atodiresei I. Asymmetrische Brønsted-Säure-katalysierte Cycloadditionen - effiziente enantioselektive Synthese von Pyrazolidinen, Pyrazolinen und 1,3-Diaminen ausN-Acylhydrazonen und Alkenen Angewandte Chemie. 124: 13036-13040. DOI: 10.1002/Ange.201205813  0.523
2011 Dufour J, Maji MS, Bolte M. (9R,10R,10aR)-9-(2-Bromo-phen-yl)-10-nitro-6-phenyl-10,10a-dihydro-9H-benzo[c]chromene-8-carbaldehyde. Acta Crystallographica. Section E, Structure Reports Online. 67: o2844. PMID 22219887 DOI: 10.1107/S160053681103995X  0.323
2010 Maji MS, Murarka S, Studer A. Transition-metal-free Sonogashira-type coupling of ortho-substituted aryl and alkynyl Grignard reagents by using 2,2,6,6-tetramethylpiperidine-N-oxyl radical as an oxidant. Organic Letters. 12: 3878-81. PMID 20704186 DOI: 10.1021/Ol1015702  0.769
2010 Maji MS, Pfeifer T, Studer A. Transition-metal-free synthesis of conjugated polymers from bis-Grignard reagents by using TEMPO as oxidant. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 5872-5. PMID 20411549 DOI: 10.1002/Chem.201000236  0.497
2010 Studer A, Maji M, Murarka S. Metal-Free Coupling of Aryl and Alkynyl Grignard Reagents Mediated by TEMPO Synfacts. 2010: 1401-1401. DOI: 10.1055/S-0030-1258861  0.71
2009 Maji MS, Studer A. Transition-metal-free oxidative homocoupling of aryl, alkenyl, and alkynyl Grignard reagents with TEMPO Synthesis. 2467-2470. DOI: 10.1055/S-0029-1216859  0.533
2009 Maji MS, Studer A. ChemInform Abstract: Transition-Metal-Free Oxidative Homocoupling of Aryl, Alkenyl, and Alkynyl Grignard Reagents with TEMPO. Cheminform. 40. DOI: 10.1002/chin.200950042  0.424
2008 Maji MS, Pfeifer T, Studer A. Oxidative homocoupling of aryl, alkenyl, and alkynyl Grignard reagents with TEMPO and dioxygen. Angewandte Chemie (International Ed. in English). 47: 9547-50. PMID 18980168 DOI: 10.1002/Anie.200804197  0.5
2008 Maji MS, Fröhlich R, Studer A. Desymmetrization of metallated cyclohexadienes with chiral N-tert-butanesulfinyl imines. Organic Letters. 10: 1847-50. PMID 18396894 DOI: 10.1021/Ol800478Q  0.549
2008 Maji M, Pfeifer T, Studer A. Oxidative Homokupplung von Aryl-, Alkenyl- und Alkinyl-Grignard-Reagentien mit TEMPO und Sauerstoff Angewandte Chemie. 120: 9690-9692. DOI: 10.1002/Ange.200804197  0.472
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