CONVENTIONAL SYNTHESIS AND STRUCTURAL ELUCIDATION OF NEWER 1,3,4-OXADIAZOLE DERIVATIVES BIO FUNCTIONING AS ANTI-BACTERIAL AND ANTI-FUNGAL

A series of newer 1,3,4-oxadiazole derivatives containing R-phenyl moiety were synthesized by reacting R-substituted aromatic acids with hydrazine hydrate in presence of various reagents at different reaction conditions. The structural elucidation of these compounds is based on their spectral data (IR, 1H NMR, MS and elemental analysis). All the newly Synthesized 1,3,4-oxadiazole derivatives have been screened for their antibacterial activity against three different strains, namely E. coli, S. aureus and P. aeruginosa, while antifungal activity was determined against three different strains such as C. neoformans, C. albicans and C.glabrata. The investigation of antimicrobial screening revealed that compounds 4a, 4g, and 4h exhibited excellent activity when compared with the standard drugs.

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-02-27
DOI
https://doi.org/10.5281/zenodo.14940193
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
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article

CONVENTIONAL SYNTHESIS AND STRUCTURAL ELUCIDATION OF NEWER 1,3,4-OXADIAZOLE DERIVATIVES BIO FUNCTIONING AS ANTI-BACTERIAL AND ANTI-FUNGAL

Zenodo (CERN European Organization for Nuclear Research)
Synthesis and biological activity
article

CONVENTIONAL SYNTHESIS AND STRUCTURAL ELUCIDATION OF NEWER 1,3,4-OXADIAZOLE DERIVATIVES BIO FUNCTIONING AS ANTI-BACTERIAL AND ANTI-FUNGAL

article en

Abstract

A series of newer 1,3,4-oxadiazole derivatives containing R-phenyl moiety were synthesized by reacting R-substituted aromatic acids with hydrazine hydrate in presence of various reagents at different reaction conditions. The structural elucidation of these compounds is based on their spectral data (IR, 1H NMR, MS and elemental analysis). All the newly Synthesized 1,3,4-oxadiazole derivatives have been screened for their antibacterial activity against three different strains, namely E. coli, S. aureus and P. aeruginosa, while antifungal activity was determined against three different strains such as C. neoformans, C. albicans and C.glabrata. The investigation of antimicrobial screening revealed that compounds 4a, 4g, and 4h exhibited excellent activity when compared with the standard drugs.

Zenodo (CERN European Organization for Nuclear Research)
Royal Pharmaceutical Society (GB)
Openalex Percentile: Top 63%
Synthesis and biological activity
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