93. Roy. M.; Mishra. B.; Maji. S.; Sinha. A.; Dutta. S.; Mondal. S.; Banerjee. A.; Pachfule. P.*; Adhikari. D.*; Covalent Organic Framework Catalyzed Amide Synthesis Directly from Alcohol Under Red Light Excitation. Angew. Chem. Int. Ed. 2024, 136, e202410300.
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92. Mishra. B.; Maji. S.; Roy. M.; Dutta. S.; Sinha. A.; Das. N.T.; Mondal. S.; Banerjee. A.; Thomas. A.; Pachfule. P.*; Adhikari. D.*; A Thiazole-Linked Dithiophenedione-Functionalized Covalent Organic Framework for Photocatalytic Oxidative Dehydrogenation Reactions. Chem. Mater. 2025, 37, 21, 8775–8786
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91. Singh. R.; Singh. V.; Nielsen. R. K. T.; Kundu. A.; Mossin. S.; Adhikari. D*.; Redox Noninnocence of a β-Diketiminate Enabling Electron Transfer Catalysis. Angew. Chem. Int. Ed. 2025, e202513087.
90. Saha. A.; Roy. M.; Maji. S.; Rana. G.; Maiti. D.*; Adhikari. D.*; Consecutive Multiphoton-Mediated Defluorinative Amination of Fluoroarenes. J. Am. Chem. Soc. 2025, 147, 20735−20747.
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89. Banerjee. R.; Roy. M.; Aggarwal. Medha.; Maji. S.; Adhikari. D*.; Mukherjee. P*.; Transformation of a Pd6 trifacial barrel to a Pd8 tetrafacial barrel by C70 as guest and oxidative photolysis of alkenes using the C70 encapsulated barrel under red light. Chem. Sci. 2025
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88. Biswas. A.; Mandal. S.; Halder. S.; Mandal. B.; Adhikari. D*.; Ligand-assisted nickel catalysis enabling N,N-dialkylation and cyclization of acyl hydrazides using aliphatic alcohols. Catal. Sci. Technol. 2025.
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87. Maji. S.; Roy. M.; Adhikari. D*.; (E)-Selective Olefination by a Cofactor-Inspired Quinone Catalysis. ChemCatChem 2025, e00544.
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86. Halder. S.; Mandal. S.; Adhikari.D*.; Direct Photoinduced Heck-Type Cyclization of Aryl Halides toward Polycyclic Indoles.
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Org. Lett. 2025, 27, 17, 4513–4518
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85. Mandal. S.; Halder. S.; Mandal. S.; Somnath. P.; Biswas. A.; Adhikari.D*.; Sustainable photocatalytic synthesis of multisubstituted quinazoline
and quinolines by naphthalene diimide. Adv. Synth. Catal. 2025, 367, e202500109.​​
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84. Alam. A.; Roy. M.; Maji. S.; Chakraborty. A.; Singh. V.; Kumar. A.; Mondal. S.; Banerjee. A.; Kailasam. K.; Adhikari. D*.; Pachufle.P*.; Xantphos– Cu-Decorated Covalent Organic Frameworks for C─H Arylation through Sensitized Electron Transfer. Adv. Mater. 2025, 2416100.
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83. Bains. A.; Jain. H.; Kundu. A.; Singh. R.; Yadav. S.; Yadav. A.; Adhikari. D.*; Cofactor-inspired quinone catalysis following a one- electron hydrogen atom transfer pathway. ACS Catal. 2024, 14, 23, 17993–18002.
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82. Bains. A.; Kundu. A.; Singh. R.; Jain. H.; Adhikari. D.*; Radical-driven imine hydrogenation promoted by the cooperativity of nickel and a redox-active ligand. Eur. J. Inorg. Chem., 2024, e202400558.
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81. Adhikari.D.; Dongbang. Sun.; Jiang. X.; Muniz. D.; Shinning light on organometallic chemistry. Organometallics 2024, 43, 1659-1661.
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80. Baguli.S.; Nath. S.; Kundu. A.; Menon. H.; Adhikari. D.*; Mukherjee. D.*; (CAAC)CuCl: A Competent Precatalyst for Carbonyl and Ester Hydrosilylation. Inorg. Chem. 2024, 63, 18552−18562.
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79. Chakraborty. A.; Roy. M.; Alam. A.; Adhikari. D.*; Pachfule. P.*; Covalent organic frameworks as heterogeneous photocatalysts for cross-coupling reactions. Green Chem., 2024, 26, 9619-9651.
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78. Singh. V.; Sinha.N.; Adhikari. D.*; Photochemical pincer-catalyzed reductive cyclization towards indolines and oxindoles.
Chem. Commun., 2024, 60, 9542-9545. (Contributed to ChemComm's 60th anniversary).
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77. Roy. M.; Mishra. B.; Maji. S.; Sinha. A.; Dutta.S.; Mondal. S.; Banerjee. A.; Pachfule. P.*; Adhikari. D.*; Covalent Organic Framework
Catalyzed Amide Synthesis Directly from Alcohol Under Red Light Excitation. Angew. Chem. Int. Ed., 2024, e202410300.
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76. Singh. V.; Kundu. A.; Weisser. K.; Hazari. A. S.; Adhikari. D.*; Exclusively Ligand-Redox-Promoted C−H Tertiary Alkylation of Heteroarenes. ACS Catal., 2024, 14, 8939–8948.
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75. Bansal. S.; Biswas. A.; Kundu. A.; Adhikari. M.; Singh. S.*; Adhikari. D.*; Ambiphilic Alcohol Dehydrogenation by BICAAC Mimicking Metal-Ligand Cooperativity. ACS Catal., 2024, 14, 8087–8095.
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74. Mandal. B.; Mandal. S.; Halder. S.; Adhikari. D.*; Photocatalytic α-arylation of cyclic ketones by a thermally activated delayed fluorescence molecule. Chem. Commun., 2024, Advance Article.
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73. Biswas. A.; Mandal. S.; Halder. S.; Singh. R.; Adhikari. D.*; Photochemical dehydrogenative transformation to heterocycles facilitated by azo/hydrazo redox couple. Catal. Sci. Technol., 2024, 14, 2146-2152.
72. Das. K.; Kundu. A.; Sarkar. K.; Adhikari. D.*; Maji. B.*; Catalytic acceptorless dehydrogenative borylation of styrenes enabled by a molecularly defined manganese complex. Chem. Sci. 2024, 15, 1098-1105.
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71. Kundu. A.; Mandal. B.; Maji. B.; Adhikari. D.*; DFT-Guided Mechanistic Insights into Chemodivergence: A Mixed Explicit– Implicit Solvent Description to Dictate the Chemoselectivity. J. Phys. Chem. A. 2023, 127, 10068-10074.
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70. Singh, V.; Jain, H.; Nath. S.; Adhikari. D.*; Multielectron Redox Afforded by a Pincer Ligand Promoting Kumada Cross- Coupling Reactions. Chem. Eur. J., 2023, e202303189.
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69. Mandal. B.; Bains. A. K.; Roy. M.; Adhikari. D.*; Photochemical oxidative dehydrogenation of saturated N-heterocycles by an iminoquinone. Catal. Sci. Technol. 2023, 13, 6512-6518.
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68. Halder. S.; Mandal. S.; Kundu. A.; Mandal. B.; Adhikari. D.*; Super-Reducing Behavior of Benzo[b]phenothiazine Anion under Visible-light Photoredox Condition. J. Am. Chem. Soc., 2023, 145, 22403-22412.
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67. Maji. S.; Roy. M.; Shaikh. K.; Adhikari. D.*; Organophotocatalytic dehydrogenative preparation of amides directly from alcohols. Green Chem., 2023, 25, 8019-8025.
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66. Dey. D.; Kundu. A.; Singh. V.; Roy. M.; Maji. S.; Adhikari. D.*; Single electron transfer catalysis by diphenylthiourea under visible light photoredox conditions. Org. Chem. Front., 2023, 10, 5248-5253.
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65. Bains. A.; Kundu. A.; Adhikari. D.*; Mechanistic Elucidation of a Radical-Promoted Hydrogenation Relevant to Borrowing Hydrogen Catalysis. ChemCatChem., 2023, 15, e202300586. (Selected as 'hot' article)
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64. Mandal, C.; Kundu, A.; Das. S.; Adhikari. D.*; Mukherjee. D.* ; A 2-Anilidomethylpyridine Ligand Framework Showcasing Hydride Storage and Transfer Abilities in Its Aluminum Chemistry. Chem. Eur. J., 2023, 29, e2023011.
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63. Baguli, S.; Kundu, A.; Nath. S.; Adhikari. D.*; Mukherjee. D.* ; A Donor–Acceptor Cyclopropane by Intramolecular C(sp3)–H Activation at a Cyclic(alkyl)(amino)carbene Center and Its Fascinating Ring-Opening Chemistry. Org. Lett., 2023, 25, 3141- 3145.
62. Singh, V.; Singh, R.; Hazari A. S.; Adhikari. D.* Unexplored facet of pincer ligand : super-reductant behavior applied to transition-metal-free catalysis. JACS Au, 2023, 3, 1213-1220.
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61. Singh, R.; Bains, A.; Kundu, A.; Jain, H. ; Yadav, S.; Dey, D.; Adhikari. D.* Mechanistic Elucidation of an Alcohol Oxidation Reaction Promoted by Nickel Azophenolate Complex. Organometallics, 2023, 42, 1759-1765.
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60. Halder. S.; Mandal. S.; Biswas. A.; Adhikari. D.* Unlocking the photo-dehydrogenation ability of naphthalene monoimide towards the synthesis of quinazolinones. Green Chem., 2023, 25, 2840-2845.
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59. Singh. K.; Kundu. A.; Adhikari. D.*; Ligand-Based Redox: Catalytic Applications and Mechanistic Aspects. ACS Catal. 2022, 12, 13075–13107.
58. Dey. D.; Kundu. A.; Mandal. B.; Roy. M.; Adhikari. D.*; Deciphering single electron transfer ability of fluorene under photoredox conditions. Catal. Sci. Technol. 2022, 12, 7322-7327.
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57. Bains. A.; Biswas. A.; Kundu. A.; Adhikari. D.*; Nickel-catalysis enabling α-alkylation of ketones by secondary alcohols. Adv. Synth. & Catal., 2022, 364, 2815-2821. (Highlighted as very important publication)
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56. Biswas. A.; Bains. A.; and Adhikari. D.*; Ligand-assisted nickel catalysis enabling sp3 C-H alkylation of 9H-fluorene with alcohols. Catal. Sci. Technol. 2022, 12, 4211-4216.
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55. Singh. V.; Kundu. A.; Singh. K.; and Adhikari. D.*; Redox-noninnocence of formazanate ligand applied to catalytic formation of α-ketoamides. Chem Commun. 2022, 58, 6630-6633. (Placed in “Emerging investigators Collection 2022")
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54. Singh. K.; Singh. R.; Hazari A. S. and Adhikari. D.*; Bimodal Photocatalytic Behaviour of a Zinc beta-diketiminate: Application to Trifluoromethylation Reaction. Chem Commun. 2022, 58, 4384-4387.
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53. Dey. D.; Kundu. A.; Roy. M.; Pal. S.; Adhikari. D.*; Aromatization as the driving force for single electron transfer towards C-C cross coupling reactions. Catal. Sci. Technol. 2022, 12, 1934-1940.
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52. A chapter on 'C-H Functionalization Reactions Following a Single-electron Transfer and Radical Pathway in the 'Handbook of C-H Functionalization'. (Wiley) Bains. A. K.; Adhikari. D.* 2022 Accepted (Editor: D. Maiti)
51. Bains. A. K.; Biswas A.; Adhikari. D.*; Nickel-Catalyzed Selective Synthesis of α- Alkylated Ketones via Dehydrogenative Cross-Coupling of Primary and Secondary Alcohols. Adv. Synth. & Catal., 2022, 364, 47-52.
50. Bains. A. K.; Kundu A.; Maiti D.*; Adhikari. D.*; Ligand-redox assisted nickel catalysis toward stereoselective synthesis of (n+1)-membered cycloalkanes from 1,n-diols with methyl ketones. Chem. Sci., 2021, 12, 14217-14223.
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49. Kundu. A.; Dey. D.; Pal. S.; Adhikari. D.*; Pyrazole-Mediated C−H Functionalization of Arene and Heteroarenes for Aryl− (Hetero)aryl Cross-Coupling Reactions. J. Org. Chem. 2021, 86, 15665-15673.
48. Singh. K.; Siddiqui. I.; Sridharan V; Yadav. R. A. K.; Jou. J-H.*; Adhikari. D.*; Aggregation Induced Enhanced Emission Active Zinc(II) β-diketiminate Complexes Enabling High-Performance Solution-Processable OLEDs. Inorg. Chem., 2021, 60, 19128- 19135.
47. Bains. A. K.; Ankit. Y.; Adhikari. D.*; Pyrenedione-Catalyzed α-Olefination of Nitriles under Visible-Light Photoredox Conditions. Org. Lett., 2021, 23, 2019-2023.
46. Sarkar. K.; Das. K.; Kundu. A.; Adhikari. D.*; Maji. B.*; Phosphine-Free Manganese Catalyst Enables Selective Transfer Hydrogenation of Nitriles to Primary and Secondary Amines Using Ammonia−Borane. ACS Catal., 2021, 11, 2786−2794.
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45. Singh. K.; Vidhyalakshmi S.; Adhikari. D.*; Visible light photoredox by a (ph,ArNacNac)2Zn photocatalyst: Photophysical properties and mechanistic understanding. Inorg. Chem. Front., 2021,8, 2078-2087.
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