Theoretical Study of the Chemical Reactivity of a Series of 2-(quinoline-4-yloxy)acetamide
Ehouman Jean Missa, Dembélé Georges Stéphane, Tuo Nanou Tiéba, Konaté Bibata, Soro Doh, DJE Daniel Yannik, Kodjo Charles Guillaume, Ziao Nahossé
American Journal of Chemistry, 2024, 14(1), pp. 4-12
DOI: 10.5923/j.chemistry.20241401.02
Open Access
The study of the stability and reactivity shows that compound B with a value of the energy gap of 3.749 eV is the most stable and the most electron accepting of the 2-(quinoline-4-yloxy)acetamide derivatives. Compound F, on the other hand, is the least stable and hardest of the series studied. The ...
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Synthesis, Characterization, Hirshfeld Surface Analysis and Quantum Chemical Calculations of 2-oxo-2H- Chromen-6-yl 4-Methoxybenzoate
Zakaria Koulabiga, Kouadio Honoré Yao, Akoun Abou, Abdoulaye Djandé, Michel Giorgi, Stéphane Coussan
American Journal of Organic Chemistry, 2024, 12(1), pp. 1-19
DOI: 10.5923/j.ajoc.20241201.01
Open Access
This article deals with a combined experimental and computational study of a 6-substituted coumarin derivative, namely, 2-oxo-2H-chromen-6-yl 4-methoxybenzoate (I). The compound was synthetized by
O-acetylation of 6-hydroxycoumarin with 4-methoxybenzoyl chloride in the presence of ...
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