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[1]
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A Facile Catalytic One-Pot Synthesis of Benzimidazole and Benzothiazole
Compounds using Amberlite IRA 400-Cl Resin as Green Catalyst
Asian Journal of Chemistry,
2022
DOI:10.14233/ajchem.2022.23595
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[2]
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A facile one-pot synthesis, computational and molecular docking studies of benzimidazole and benzothiazole compounds using Amberlite IRA 400-Cl resin as green/reusable catalyst
Journal of Molecular Structure,
2022
DOI:10.1016/j.molstruc.2022.133704
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[3]
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A facile one-pot synthesis, computational and molecular docking studies of benzimidazole and benzothiazole compounds using Amberlite IRA 400-Cl resin as green/reusable catalyst
Journal of Molecular Structure,
2022
DOI:10.1016/j.molstruc.2022.133704
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[4]
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A facile one-pot synthesis, computational and molecular docking studies of benzimidazole and benzothiazole compounds using Amberlite IRA 400-Cl resin as green/reusable catalyst
Journal of Molecular Structure,
2022
DOI:10.1016/j.molstruc.2022.133704
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[5]
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A 2-(benzothiazol-2-yl)-phenolato platinum(II) complex as potential photosensitizer for combating bacterial infections in lung cancer chemotherapy†
European Journal of Medicinal Chemistry,
2021
DOI:10.1016/j.ejmech.2021.113600
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[6]
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Mixed valent copper oxide nanocatalyst on Zeolite-Y for mechanochemical oxidation, reduction and C–C bond formation reaction
Microporous and Mesoporous Materials,
2021
DOI:10.1016/j.micromeso.2021.111392
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[7]
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Mixed valent copper oxide nanocatalyst on Zeolite-Y for mechanochemical oxidation, reduction and C–C bond formation reaction
Microporous and Mesoporous Materials,
2021
DOI:10.1016/j.micromeso.2021.111392
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[8]
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Exploring beta amyloid cleavage enzyme‐1 inhibition and neuroprotective role of benzimidazole analogues as anti‐alzheimer agents
Journal of the Chinese Chemical Society,
2020
DOI:10.1002/jccs.201900200
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[9]
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Aerobic {Mo72V30} nanocluster‐catalysed heterogeneous one‐pot tandem synthesis of benzimidazoles
Applied Organometallic Chemistry,
2019
DOI:10.1002/aoc.4638
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[10]
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Facile Sol-Gel Synthesis of Co3O4 Nanoparticles — An Efficient and Recyclable Catalyst for the Synthesis of 1,2-Disubstituted Benzimidazoles Under Solvent-Free Conditions
Russian Journal of Organic Chemistry,
2019
DOI:10.1134/S1070428019080220
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[11]
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Exploring beta amyloid cleavage enzyme‐1 inhibition and neuroprotective role of benzimidazole analogues as anti‐alzheimer agents
Journal of the Chinese Chemical Society,
2019
DOI:10.1002/jccs.201900200
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[12]
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Aerobic {Mo
72
V
30
} nanocluster‐catalysed heterogeneous one‐pot tandem synthesis of benzimidazoles
Applied Organometallic Chemistry,
2018
DOI:10.1002/aoc.4638
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[13]
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Copper containing nanosilica thioalated dendritic material: A recyclable catalyst for synthesis of benzimidazoles and benzothiazoles
Applied Organometallic Chemistry,
2018
DOI:10.1002/aoc.3937
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[14]
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Magnetic Co‐doped NiFe2O4 Nanocomposite: A Heterogeneous and Recyclable Catalyst for the One‐Pot Synthesis of Benzimidazoles, Benzoxazoles and Benzothiazoles under Solvent‐Free Conditions
Journal of the Chinese Chemical Society,
2017
DOI:10.1002/jccs.201700060
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[15]
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Magnetic Co-doped NiFe2
O4
Nanocomposite: A Heterogeneous and Recyclable Catalyst for the One-Pot Synthesis of Benzimidazoles, Benzoxazoles and Benzothiazoles under Solvent-Free Conditions
Journal of the Chinese Chemical Society,
2017
DOI:10.1002/jccs.201700060
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[16]
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Copper containing nanosilica thioalated dendritic material: A recyclable catalyst for synthesis of benzimidazoles and benzothiazoles
Applied Organometallic Chemistry,
2017
DOI:10.1002/aoc.3937
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[17]
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Synthesis of benzimidazole and quinoxaline derivatives using reusable sulfonated rice husk ash (RHA-SO3H) as a green and efficient solid acid catalyst
Research on Chemical Intermediates,
2016
DOI:10.1007/s11164-015-2075-5
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[18]
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Diversity Oriented Synthesis of Indoloazepinobenzimidazole and Benzimidazotriazolobenzodiazepine fromN1-Alkyne-1,2-diamines
Chemistry - A European Journal,
2015
DOI:10.1002/chem.201502956
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[19]
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Diversity Oriented Synthesis of Indoloazepinobenzimidazole and Benzimidazotriazolobenzodiazepine from N1‐Alkyne‐1,2‐diamines
Chemistry – A European Journal,
2015
DOI:10.1002/chem.201502956
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