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              <text>Catalytic potential of fluorescein under visible light irradiation: Enabling single-pot open flask synthesis of novel pyrazolyl methanesulfonamides</text>
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              <text>Five-component; Multicomponent; Pyrazolyl methanesulfonamide; Single-pot; Visible light irradiated</text>
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              <text>This groundbreaking study introduces a novel and efficient method for synthesizing a range of substituted pyrazolyl methanesulfonamides through a five-component cyclocondensation reaction. This reaction incorporates five different components, such as ethyl acetoacetate, hydrazine, dimedone, benzaldehydes, substituted phenyl acetonitriles, and methyl sulfonyl chloride was made to react under visible light irradiation, with fluorescein serving as an effective catalyst and ethanol as solvent for 30 mintues. This method offers significant advantages, including simplified handling, higher yields of target products with shorter reaction times, and easier purification processes. We successfully synthesized around 15 novel pyrazolyl methanesulfonamide derivatives with high efficiency. Comprehensive spectral characterization confirmed the structural integrity and purity of these derivatives, demonstrating the robustness and versatility of this approach. Facilitated by visible light and utilizing fluorescein as a bio-friendly catalyst, this methodology is both green and sustainable. This innovative approach not only streamlines the synthesis of pyrazolyl methanesulfonamides but also holds considerable promise for advancing research and applications in fields such as medicinal chemistry and materials science.  2024 The Author(s)</text>
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              <text>Kumar S L.; Ramaraj S.G.; Tabassum S.; Chundattu S.J.; Govindaraju S.</text>
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              <text>Journal of Organometallic Chemistry, Vol-1025</text>
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              <text>Elsevier B.V.</text>
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              <text>2025-01-01</text>
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              <text>&lt;a href="https://doi.org/10.1016/j.jorganchem.2024.123476" target="_blank" rel="noreferrer noopener"&gt;https://doi.org/10.1016/j.jorganchem.2024.123476&lt;/a&gt;
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              <text>All Open Access; Hybrid Gold Open Access</text>
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              <text>ISSN: 0022328X; CODEN: JORCA</text>
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              <text>Kumar S L., Department of Chemistry, Christ University, Bengaluru, 570029, India; Ramaraj S.G., Department of Bioengineering, of Engineering, The University of Tokyo, 7-3-1 Hongo, Japan, Department of Materials Physics, Saveetha School of Engineering, Saveetha Institute of Medical and Technical Sciences (SIMTS), Thandalam, Tamilnadu, Chennai, 602105, India; Tabassum S., Department of Chemistry, Surana College - Autonomous, South End Road, Bengaluru, Basavanagudi, 560004, India; Chundattu S.J., Department of Sciences and Humanities, Christ University, Bengaluru, 570074, India; Govindaraju S., Department of Sciences and Humanities, Christ University, Bengaluru, 570074, India</text>
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