Design and synthesis of various 1,3,4-oxadiazoles as AChE and LOX enzyme inhibitors
N-Substituted-2-propanamide analogues of 1,3,4-oxadiazole have been synthesized using a multi-step synthetic protocol to explore new therapeutic anti-enzymatic agents. Herein, we have merged sulfonyl, piperidine, oxadiazole and amide into a single unit to synthesize a library of unique compounds, 8a...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
De Gruyter
2023-11-01
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| Σειρά: | Heterocyclic Communications |
| Θέματα: | |
| Διαθέσιμο Online: | https://doi.org/10.1515/hc-2022-0169 |
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