has been cited by the following article(s):
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[1]
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Sustainable synthesis of 1, 8-dioxooctahydroxanthenes in deep eutectic solvents (DESs)
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2021 |
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[2]
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Green protocol for the synthesis of 1, 8-dioxo-decahydroacridines via Hantzsch condensation using citric acid as organocatalyst
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2019 |
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[3]
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Carbon-based nanocatalyst: An efficient and recyclable heterogeneous catalyst for one-pot synthesis of gem-bisamides, hexahydroacridine-1,8-diones and 1,8-dioxo …
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2019 |
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[4]
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Green protocol for the synthesis of 1, 8-dioxo-decahydroacridines by Hantzsch condensation using citric acid as organocatalyst
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2019 |
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[5]
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Nickel NPs @N-doped titania: an efficient and recyclable heterogeneous nanocatalytic system for one-pot synthesis of pyrano[2,3-d]pyrimidines and 1,8-dioxo …
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2019 |
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[6]
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Green protocol for the synthesis of 1, 8-dioxo-decahydroacridines by Hantzsch condensation using citric acid as organocatalyst.
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2019 |
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[7]
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Uses of dimedone for the synthesis of new heterocyclic derivatives with anti-tumor, c-Met, tyrosine, and Pim-1 kinases inhibitions
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Medicinal Chemistry Research,
2018 |
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[1]
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A sustainable gateway to access 1,8-dioxo-octahydroxanthene scaffolds via a surface-engineered halloysite-based magnetically responsive catalyst
New Journal of Chemistry,
2022
DOI:10.1039/D1NJ05509G
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[2]
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Sustainable synthesis of 1,8-dioxooctahydroxanthenes in deep eutectic solvents (DESs)
New Journal of Chemistry,
2021
DOI:10.1039/D1NJ00743B
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[3]
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Nickel NPs @N-doped titania: an efficient and recyclable heterogeneous nanocatalytic system for one-pot synthesis of pyrano[2,3-d]pyrimidines and 1,8-dioxo-octahydroxanthenes
Journal of the Iranian Chemical Society,
2019
DOI:10.1007/s13738-019-01669-4
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[4]
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Carbon-based nanocatalyst: An efficient and recyclable heterogeneous catalyst for one-pot synthesis of gem-bisamides, hexahydroacridine-1,8-diones and 1,8-dioxo-octahydroxanthenes
Journal of the Iranian Chemical Society,
2019
DOI:10.1007/s13738-019-01723-1
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[5]
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Uses of dimedone for the synthesis of new heterocyclic derivatives with anti-tumor, c-Met, tyrosine, and Pim-1 kinases inhibitions
Medicinal Chemistry Research,
2018
DOI:10.1007/s00044-018-2208-7
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