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• Roy. M.#,  Sen, A.#, Maji, S., Roy, Choudhury, A.*, Adhikari, D.*; HATCN as an efficient organo-photo catalyst for dehydrogenative lactonization of 2-arylbenzoic acids, manuscript under preparation., 2026. (#contributed equally)

• Sen, A.#, Roy. M.#, Maji, S., Roy, Choudhury, A.*, Adhikari, D.*; A phenanthroline based dicationic salt as a bifunctional redox catalyst: oxidative SNAr and reductive aryl halide cleavage,  manuscript under preparation., 2026. (#contributed equally)

• Roy. M.#; Saha. A.#;  Kabari. S.; Maji. S.; Maiti. D.*; Adhikari. D.*; A photocatalytic oxidative SNAr strategy for synthesis of bis-azaarenes, manuscript under revision., 2025. (#contributed equally)

• Roy. M.; Maji. S.; Singh. V.; Dey. D.; Adhikari. D*.; Dramatic expansion of bimodal redox window of indigo by 2-electron redox processes. Nat. Commun. 2025, 16, 11387.

• Dutta. S.#;  Roy. M.#; Maji. S.; Mishra. B.; Sen. A.; Tiwari. A.; Das. N. T.;  Mondal. S.; Banerjee. A.; Adhikari. D.*; Pachfule. P.*;  Cationic covalent organic framework for photocatalytic defluorinative amination of fluoroarenes.  Angew. Chem. Int. Ed. 2025, 64, e202516235. (Selected as 'hot' article), (#contributed equally)

• 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.

• Saha. A.#; Roy. M.#; Maji. S.; Rana. G.; Datta. A.; Maiti. D.*; Adhikari. D.*; Three photon absorbing photocatalyst enabled defluorinative amination of fluoroarenes. J. Am. Chem. Soc. 2025, 147, 20735−20747.  (#contributed equally)

• Banerjee. R.#; Roy. M.#; Aggarwal. M.; Maji. S.; Mukherjee. P.; 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, 16, 12885-12895. (#contributed equally)

• Alam. A.#; Roy. M.#; Maji. S.; Chakraborty. A.; Singh. V.; Kumar. A.;  Mondal. S.; Banerjee. A.; Kailasam. K.; Adhikari. D.*; Pachfule. P.*; Xantphos–Cu-decorated covalent organic frameworks for C─H arylation through sensitized electron transfer. Adv. Mater. 2025, 2416100. (#contributed equally)

• Maji. S.; Roy. M.; Adhikari. D.*;  (E)-Selective olefination by a co-factor inspired Quinone. ChemCatChem 2025, 37, e00544.

• 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.

• 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. (Selected as 'hot' article),(#contributed equally).

• Maji. S.#; Roy. M.#; Shaikh. K.; Adhikari. D.*; Organophotocatalytic dehydrogenative preparation of amides directly from alcohols. Green Chem., 2023, 25, 8019-8025. (#contributed equally)

• 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.

• 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.

• 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.

• 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.