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https://scidar.kg.ac.rs/handle/123456789/15064
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DC Field | Value | Language |
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dc.rights.license | BY-NC-ND | - |
dc.contributor.author | Bukhari, Syed Nasir Abbas | - |
dc.contributor.author | Ejaz, Hasan | - |
dc.contributor.author | Elsherif M. | - |
dc.contributor.author | Janković, Nenad | - |
dc.date.accessioned | 2022-09-13T11:51:05Z | - |
dc.date.available | 2022-09-13T11:51:05Z | - |
dc.date.issued | 2022 | - |
dc.identifier.uri | https://scidar.kg.ac.rs/handle/123456789/15064 | - |
dc.description.abstract | Dihydrouracil presents a crucial intermediate in the catabolism of uracil. The vital im-portance of uracil and its nucleoside, uridine, encourages scientists to synthesize novel dihydroura-cils. In this paper, we present an innovative, fast, and effective method for the synthesis of dihy-drouracils. Hence, under mild conditions, 3‐chloroperbenzoic acid was used to cleave the carbon– sulfur bond of the Biginelli hybrids 5,6‐dihydropyrimidin‐4(3H)‐ones. This approach led to thirteen novel dihydrouracils synthesized in moderate‐to‐high yields (32–99%). | - |
dc.rights | openAccess | - |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/ | - |
dc.source | Molecules | - |
dc.title | Synthesis and Characterization of Dihydrouracil Analogs Utilizing Biginelli Hybrids | - |
dc.type | article | - |
dc.identifier.doi | 10.3390/molecules27092939 | - |
dc.identifier.scopus | 2-s2.0-85130072798 | - |
Appears in Collections: | Institute for Information Technologies, Kragujevac |
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File | Description | Size | Format | |
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molecules-27-02939-v2.pdf | 1.21 MB | Adobe PDF | View/Open |
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