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...
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Published in | Heterocyclic Communications Vol. 29; no. 1; pp. 149 - 60 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin
Walter de Gruyter GmbH
15.11.2023
De Gruyter |
Subjects | |
Online Access | Get full text |
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