In this study, a facile and versatile procedure for the synthesis of a chalcone derivate that a functionalized (E,Z)-2-(4-aminobenzylidene)acenaphthylen-1(2H)-one, 4 was synthesized and also characterized by using FT-IR, NMR and MS. A new HPLC method for the separation of its diastereomers was developed by using a chiral column that contains the amylose tris(3,5-dimethylphenylcarbamate) as a chiral selector since it is effective, reproducible and can be used for preparative purposes. High percentage recovery claims that the presented method was not affected by the impurities in the biological media. RSD% values for the repeatability studies suggest that the optimized method was highly precise and reproducible which is very important for these promising advances, chalcone-based science is expected to be applied in drug discovery.
Chalcone; Diastereomeric separation; Acenaphtenone; Chiral column; HPLC
Birincil Dil | İngilizce |
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Konular | Analitik Kimya, Organik Kimya |
Bölüm | Kimya |
Yazarlar | |
Yayımlanma Tarihi | 30 Haziran 2021 |
Gönderilme Tarihi | 12 Mayıs 2021 |
Kabul Tarihi | 31 Mayıs 2021 |
Yayımlandığı Sayı | Yıl 2021 Cilt: 11 Sayı: 1 |
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