has been cited by the following article(s):
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[1]
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Thiochromene candidates: design, synthesis, antimicrobial potential and in silico docking study
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Journal of the Iranian Chemical Society,
2022 |
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[2]
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Design, Synthesis, and In Silico Molecular Docking Study of Some Novel Thiochromene Derivatives with Antimicrobial Potential
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Polycyclic Aromatic …,
2022 |
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[3]
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SYNTHESIS AND BIOLOGICAL EVALUATION OF NOVEL TRIAZOLYL QUINAZOLIN-4-ONE DERIVATIVES AS ANTICANCER AGENTS
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2021 |
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[4]
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Design, synthesis and molecular modeling studies of 2-styrylquinazoline derivatives as EGFR inhibitors and apoptosis inducers
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2020 |
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[5]
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Synthesis and biological evaluation of novel triazolylquinazolin‐4‐one derivatives as anticancer agents
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European Journal of Molecular & …,
2020 |
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[6]
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Solvent in Solute System for the Synthesis of Highly Substituted Pyridine by Using Choline Hydroxide and Water
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Polycyclic Aromatic Compounds,
2018 |
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[7]
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CdS nanoparticles: An efficient, clean and reusable heterogeneous catalyst for one-pot procedure for synthesis of 3, 4-Dihydropyrimidin-2 (1H)-ones in solvent-free …
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2015 |
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[8]
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CdS nanoparticles: An efficient, clean and reusable heterogeneous catalyst for one-pot procedure for synthesis of 3, 4-Dihydropyrimidin-2 (1H)-ones in solvent …
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2015 |
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[9]
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CdS nanoparticles: An efficient, clean and reusable heterogeneous catalyst for one-pot procedure for synthesis of 3, 4-Dihydropyrimidin-2 (1H)-ones in solvent-free conditions
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Int. J. Bio-Inorg. Hybr. Nanomater,
2015 |
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[10]
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Nucleotides and oligonucleotides: mononucleotides
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Organophosphorus Chemistry: Volume 44,
2015 |
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[1]
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Thiochromene candidates: design, synthesis, antimicrobial potential and in silico docking study
Journal of the Iranian Chemical Society,
2022
DOI:10.1007/s13738-021-02391-w
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[2]
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Design, synthesis and molecular modeling studies of 2-styrylquinazoline derivatives as EGFR inhibitors and apoptosis inducers
Bioorganic Chemistry,
2020
DOI:10.1016/j.bioorg.2020.104358
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[3]
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Solvent in Solute System for the Synthesis of Highly Substituted Pyridine by Using Choline Hydroxide and Water
Polycyclic Aromatic Compounds,
2018
DOI:10.1080/10406638.2018.1485713
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