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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