An efficient approach to access 2,5‐disubstituted 1,3,4‐oxadiazoles by oxidation of 2‐arenoxybenzaldehyde <i>N‐</i> acyl hydrazones with molecular iodine-Reference-Cited by-同舟云学术

An efficient approach to access 2,5‐disubstituted 1,3,4‐oxadiazoles by oxidation of 2‐arenoxybenzaldehyde N‐ acyl hydrazones with molecular iodine

Published:2022-07-08 Issue:26 Volume:7 Page:
ISSN:2365-6549
Container-title:ChemistrySelect
language:en
Short-container-title:ChemistrySelect

Author:

Başpınar Küçük Hatice¹^ORCID,Alhonaish Anoud¹,Yıldız Tülay¹^ORCID,Güzel Mustafa²³^ORCID

Affiliation:

1. Istanbul University-Cerrahpasa Faculty of Engineering Department of Chemistry, Organic Chemistry Division Avcılar/ISTANBUL 34320 Turkey

2. Istanbul Medipol University, Research Institute for Health Sciences and Technologies (SABITA) Center of Drug Discovery and Development Kavacık- Beykoz/Istanbul 34810 Turkey

3. Istanbul Medipol University, International School of Medicine, Department of Medical Pharmacology, Kavacik Campus Kavacik-Beykoz/ISTANBUL 34810 Turkey

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.202201391

Reference31 articles.

1. Inhibition of Tobacco Bacterial Wilt with Sulfone Derivatives Containing an 1,3,4-Oxadiazole Moiety

2. Synthesis and antimicrobial studies of a new series of 2-{4-[2-(5-ethylpyridin-2-yl)ethoxy]phenyl}-5-substituted-1,3,4-oxadiazoles

3. Synthesis and anticonvulsant activity of new 2-substituted-5-(2-benzyloxyphenyl)-1,3,4-oxadiazoles

4. Novel limonene and citral based 2,5-disubstituted-1,3,4-oxadiazoles: A natural product coupled approach to semicarbazones for antiepileptic activity

5. Antiallergic Activity Profile in Vitro RBL-2H3 and in Vivo Passive Cutaneous Anaphylaxis Mouse Model of New Sila-Substituted 1,3,4-Oxadiazoles

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