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# List of Publication by Dr. Laksmikanta Adak
1 Kundu, P.; Roy, K.; Saha, A.; Mondal, S.; Adak, L., Reusable, Efficient Manganese–Copper-Catalyzed Cross-Coupling of Aryl Halides with Aromatic Alcohols under Solvent-Minimized Conditions, 10, e01770, ChemistrySelect, 2025
2 Panja, S.; Paul, B.; Saha, A.; Roy, K.; Nandi, C.; Majhi, B.; Adak, L.; Ranu, B. C., Ruthenium-Catalyzed Site-Selective Annulation of Benzoxazinones: An Easy Access to Dihydroisoquinoline Benzamide Derivatives, 31, e202500512, Chem. Eur. J., 2025
3 Saha, A., Roy, K., Mondal, S., Saha, B., Sumar, J., Sahu, S. K., Adak, L., Reusable cobalt–copper-catalyzed cross-coupling of (hetero) aryl halides with primary amides under air: investigating a new Co0/CoII-based catalytic cycle, 23, 5343-5351, Org. Biomol. Chem., 2025
4 Roy, K., Saha, A., Saha, B., Banerjee, S., Mukhopadhyay, C. D., Sahu, S. K., Adak, L., Reusable Iron?Copper Catalyzed Cross?Coupling of Primary Amides with Aryl and Alkyl Halides: Access to N?Arylamides as Potential Antibacterial and Anticancer Agents, 31, e202403649, Chem. Eur. J., 2025
5 Mondal, S.; Roy, K.; Pramanik, P.; Sahoo, S.; Kundu, P.; Saha, A.; Mondal, R.; Adak, L., Sustainable Mn-Assisted Cu-Catalyzed Cross-Coupling of Primary Amides and Sulfonamides with (Hetero)Aryl and Styryl Halides: Investigating a Novel Catalytically Active Species, doi.org/10.1002/asia.202500764, Chem Asian J., 2025
6 Sahoo, S.; Mandal, A.; Patra, A.; Adak, L., Palladium-Catalyzed Decarboxylative Cross-Coupling of 2,4-Dienoic Acids and Aryl Halides: Access to Fluorescence Active (E,E)?1,4- Diarylbutadienes, https://doi.org/10.1021/acs.joc.5c00782, J. Org. Chem., 2025
7 Saha, A.; Roy, K.; Banerjee, S.; Panja, S.; Khatua, M.; Mukhopadhyay; C. M., Samanta, S.; Adak, L., Room temperature palladium-catalyzed synthesis of novel unsymmetrical diamide scaffolds containing moieties of ?-ketoester as potential antibacterial, antifungal and anticancer Agents, 1322, 140177, Journal of Molecular Structure, 2025
8 Patel,A. R.; Maity, G.; Pati, T. K.; Adak, L.; Cioffi, C. L.; Banerjee, S., Hybrid Pd0.1Cu0.9Co2O4 nano-flakes: a novel, efficient and reusable catalyst for the one-pot heck and Suzuki couplings with simultaneous transesterification reactions under microwave irradiation, 12, 1496234, Frontiers in Chemistry, 2024
9 Roy, K.; Saha, A.; Sahoo, S.; Banerjee, Chitrangada Das Mukhopadhyay, Banerjee, S.; Adak, L., Reaction under Ball-Milling: Solvent-and Metal-Free One-Pot Diastereoselective Synthesis of Tetrahydroquinoline Derivatives as Potential Antibacterial and Anticancer Agents, 35, 2487-2495, Synlett, 2024
10 Roy, K.; Sahoo, S.; Saha, A.; Adak, L., Ball milling in organic transformations, 27, 153-165, Curr. Org. Chem., 2023
11 Ranu, B. C.; Adak, L.; Mukherjee, N.; Ghosh, T., Benign-Metal-Catalyzed Carbon–Carbon and Carbon–Heteroatom Bond Formation, 34, 601-621, Synlett, 2023
12 Ranu, B. C.; Adak, L.; Mukherjee, N.; Ghosh, T., Benign-Metal-Catalyzed Carbon–Carbon and Carbon–Hetero¬atom Bond Formation, DOI: 10.1055/a-1904-0152, Synlett, 2022
13 Adak, L.; Kundu, D.; Roy, K.; Saha, M.; Roy, A., Reusable Iron/Iron Oxide-Based Nanoparticles Catalyzed Organic Reactions, 26, 399-417, Curr. Org. Chem., 2022
14 Ranu, B. C.; Adak, L.; Ghosh, T., Learning Green Chemistry and its principles from Nature’s process and development of green procedures mimicking nature, 4, 127-141, Chemistry Teacher International, 2022
15 Adak, L.; Hatakeyama, T.; Nakamura, M., Iron-Catalyzed Cross- Coupling Reactions Tuned by Bulky ortho-Phenylene Bisphosphine Ligands, 94, 1125–1141, Bull. Chem. Soc. Jpn., 2021
16 Adak, L.; Jin, M.; Saito, S.; Kawabata, T.; Itoh, T.; Ito, S.; Sharma, A. K.; Isozaki, K. Nakamura, M., Iron-Catalysed Enantioselective Carbometalation of Azabicycloalkenes, 57, 6975–6978, Chem. Commun., 2021
17 Ranu, B. C.; Ghosh, T.; Adak, L., Recent Progress on Carbon-Chalcogen Bond Formation Reaction Under Microwave Irradiation, 7, 40-49, Curr. Microwave Chem., 2020
18 Adak, L.; Ghosh, T., Recent Progress in Iron-Catalyzed Reactions towards the Synthesis of Bioactive Five- and Six-Membered Heterocycles, 24, 2634-2664, Curr. Org. Chem., 2020
19 Iwamoto, T.; Okuzono, C.; Adak, L.; Jin, M. Nakamura, M., Iron-Catalysed Enantioselective Suzuki–Miyaura Coupling of Racemic Alkyl Bromides, 55, 1128–1131, Chem. Commun., 2019
20 Sharma, A. K.; Sameera, W. M. C.; Jin, M.; Adak, L.; Okuzono, C.; Iwamoto, T.; Kato, M.; Nakamura, M.; Morokuma, K., DFT and AFIR Study on the Mechanism and the Origin of Enantioselectivity in Iron- Catalyzed Cross-Coupling Reactions, 139, 16117– 16125, J. Am. Chem. Soc., 2017
21 Adak, L.; Kawamura, S.; Toma, G.; Isozaki, K.; Takaya, H.; Orita, A.; Li, H. C.; Nakamura, M., Synthesis of Aryl C-Glycosides via Iron-Catalyzed Cross-Coupling of Halosugars: Stereoselective Anomeric Arylation of Glycosyl Radicals, 139, 10693– 10701, J. Am. Chem. Soc., 2017
22 Takaya, H.; Nakajima, S.; Nakagawa, N.; Isozaki, K.; Imayoshi, R.; Gower, N. J.; Adak, L.; Hatakeyama, T.; Honma, T.; Nagashima, H.; Nakamura, M., Investigation of Organoiron Catalysis in Kumada–Tamao–Corriu-Type Cross-Coupling Reaction Assisted by Solution-Phase X-ray Absorption Spectroscopy, 88, 410– 418, Bull. Chem. Soc. Jpn., 2015
23 Jin, M.; Adak, L.; Nakamura, M., Iron-Catalyzed Enantioselective Cross- Coupling Reactions of ?- Chloroesters with Aryl Grignard Reagents, 137, 7128– 7134, J. Am. Chem. Soc., 2015
24 Jin, M.; Adak, L.; Nakamura, M., Iron-Catalyzed Enantioselective Coupling of ?-Chloroesters, 11, 0861-0861, Synfacts, 2015
25 Banerjee, S.; Adak, L.; Ranu, B. C., Ionic Liquid/PPh3 Promoted Cleavage of Diphenyl Disulfide and Diselenide: A Straight–Forward One-Pot Route to the Synthesis of Unsymmetrical Sulfides and Selenides, 53, 2149– 2152, Tetrahedron Lett., 2012
26 Saha, D.; Adak, L. ; Ranu, B. C., Hydroxyapatite-Supported Cu(I)-Catalysed Cyanation of Styrenyl Bromides with K4[Fe(CN)6]: an Easy Access to Cinnamonitriles, 10, 952– 957, Org. Biomol. Chem., 2012
27 Adak, L.; Yoshikai, N., Iron-Catalyzed Annulation Reaction of Arylindium Reagents and Alkynes to Produce Substituted Naphthalenes, 68, 5167– 5171, Tetrahedron, 2012
28 Bhadra, S.; Adak, L.; Samanta, S.; Islam, A. K. M. M.; Mukherjee, M.; Ranu, B. C., Synthesis of Oxazines and Dioxanes from Aziridines and Epoxides, 3, 0339-0339, Synfacts, 2011
29 Adak, L.; Bhadra, S.; Chattopadhyay, K.; Ranu, B. C., Amphiphilic Allylation of Activated Alkenes by Allyl Acetates and Allylstannanes Catalyzed by Palladium Nanoparticles, 35, 430– 437, New J. Chem., 2011
30 Adak, L.; Chan, W. C.; Yoshikai, N., Nickel-Catalyzed, Directing Group-Assisted [2+2+2] Cycloaddition of Imine and Alkynes, 6, 359– 362, Chem. Asian J., 2011
31 Adak, L.; Yoshikai, N., Cobalt-Catalyzed Preparation of Arylindium Reagents from Aryl and Heteroaryl Bromides, 76, 7563– 7568, J. Org. Chem., 2011
32 Saha, D.; Adak, L.; Ranu, B. C., Palladium(0) Nanoparticles- Catalyzed Ligand–free Direct Arylation of Benzothiazoles via C-H Bond Functionalization, 51, 5624– 5627, Tetrahedron Lett., 2010
33 Adak, L.; Bhadra, S.; Ranu, B. C., Palladium (0) Nanoparticle– Catalyzed sp2 C–H Activation: A Convenient Route to Alkyl–Aryl Ketones by Direct Acylation of Aryl Bromides and Iodides with Aldehydes, 51, 3811– 3814, Tetrahedron Lett., 2010
34 Bhadra, S.; Adak, L. ; Samanta, S.; Islam, A. K. M. M.; Mukherjee, M.; Ranu, B. C., Alumina-Supported Cu (II), A Versatile and Recyclable Catalyst for Regioselective Ring Opening of Aziridines and Epoxides and Subsequent Cyclization to Functionalized 1,4-Benzoxazines and 1,4- Benzodioxanes, 75, 8533– 8541, J. Org. Chem., 2010
35 Ranu, B. C.; Chatopadhyay, K.; Adak, L.; Saha, A.; Bhadra, S.; Saha, D.; Dey, R., Metal Nanoparticles as Efficient Catalysts for Organic Reactions, 81, 2337– 2354, Pure Appl. Chem., 2009
36 Adak, L.; Chattopadhyay, K.; Ranu, B. C., C—N Bond Formation with Palladium Nanoparticles, 8, 0937-0937, Synfacts, 2009
37 Adak, L.; Chattopadhyay, K.; Ranu, B. C., Palladium Nanoparticles– Catalyzed C–N Bond Formation. A Highly Regio–and Stereoselective Allylic Amination by Allyl Acetates, 74, 3982– 3985, J. Org. Chem., 2009
38 Ranu, B. C.; Bhadra, S.; Adak, L., Indium (III) Chloride- Catalyzed Oxidative Cleavage of Carbon-Carbon Multiple Bonds by tert-Butyl Hydroperoxide in Water a Safer Alternative to Ozonolysis, 49, 2588– 2591, Tetrahedron Lett., 2008
39 Ranu, B. C.; Adak, L.; Banerjee, S., Ionic Liquid Promoted Interrupted Feist–Benary Reaction with High Diastereoselectivity, 49, 4613– 4617, Tetrahedron Lett., 2008
40 Samanta, S.; Adak, L.; Jana, R.; Mostafa, G.; Tunonen, H. M.; Ranu, B. C.; Goswami, S., Oxidative ortho-C–N Fusion of Aniline by OsO4. Isolation, Characterization of Oxo–Amido Osmium(VI) Complexs, and their Catalytic Activities for Oxidative C–C Bond Cleavage of Unsaturated Hydrocarbons, 47, 11062– 11070, Inorg. Chem., 2008
41 Ranu, B. C.; Adak, L.; Chattopadhyay, K., Hydroxyapatite–Supported Palladium–Catalyzed Efficient Synthesis of (E)-2- Alkene-4-ynecarboxylic Esters, Intense Fluorescence Emission of Selected Compounds, 73, 5609– 5612, J. Org. Chem., 2008
42 Ranu, B. C.; Adak, L.; Banerjee, S., Efficient Regio– and Stereo– Selective Cleavage of Aziridines and Epoxides using an Ionic Liquid as Reagent and Reaction Medium, 85, 366–371, Can. J. Chem., 2007
43 Ranu, B. C.; Adak, L.; Banerjee, S., Halogenation of Carbonyl Compounds by an Ionic Liquid, [AcMIm]X, and Ceric Ammonium Nitrate (CAN), 60, 358– 362, Aust. J. Chem., 2007
44 Ranu, B. C.; Banerjee, S.; Adak, L., Regioselective Cross– Coupling of Allylindium Reagents with Activated Benzylic Bromides-A Simple and Efficient Procedure for the Synthesis of Terminal Alkenes, 48, 7374– 7379, Tetrahedron Lett., 2007
45 Ranu, B. C.; Chattopadhyay, K.; Adak, L., Solvent-Controlled Highly Selective Bis– and Monoallylation of Active Methylene Compounds by Allyl Acetate with Palladium(0)Nanoparticle, 9, 4595– 4598, Org. Lett., 2007

Created: 23 November 2019