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• W2913841166 abstract "4-Oxoquinolines are a class of organic substances of great importance in medicinal chemistry, due to their biological and synthetic versatility. N -1-Alkylated-4-oxoquinoline derivatives have been associated with different pharmacological activities such as antibacterial and antiviral. The presence of a carboxamide unit connected to carbon C-3 of the 4-oxoquinoline core has been associated with various biological activities. Experimentally, the N-ethylation reaction of N -benzyl-4-oxo-1,4-dihydroquinoline-3-carboxamide occurs at the nitrogen of the oxoquinoline group, in a regiosselective way. In this work, we employed DFT methods to investigate the regiosselective ethylation reaction of N -benzyl-4-oxo-1,4-dihydroquinoline-3-carboxamide, evaluating its acid/base behavior and possible reaction paths." @default.
• W2913841166 created "2019-02-21" @default.
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• W2913841166 date "2019-02-12" @default.
• W2913841166 modified "2023-10-16" @default.
• W2913841166 title "Study on the regioselectivity of the N-ethylation reaction of <i>N</i>-benzyl-4-oxo-1,4-dihydroquinoline-3-carboxamide" @default.
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• W2913841166 doi "https://doi.org/10.3762/bjoc.15.35" @default.
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