دورية أكاديمية

Synthesis and Investigation of Antimicrobial and Antioxidant Activity of 3-Nitro-N- (3-chloro-2-oxo-substituted-phenyl-azetidin-1-yl)naphtho [2,1-b]furan-2-carboxamides

التفاصيل البيبلوغرافية
العنوان: Synthesis and Investigation of Antimicrobial and Antioxidant Activity of 3-Nitro-N- (3-chloro-2-oxo-substituted-phenyl-azetidin-1-yl)naphtho [2,1-b]furan-2-carboxamides
المؤلفون: K. Shashikala Devi, M. Ramaiah, D. L. Roopa, V. P. Vaidya
المصدر: E-Journal of Chemistry, Vol 7, Iss S1, Pp S358-S362 (2010)
بيانات النشر: Wiley, 2010.
سنة النشر: 2010
المجموعة: LCC:Chemistry
مصطلحات موضوعية: Chemistry, QD1-999
الوصف: Ethyl-3-nitronaphtho[2,1-b]furan-2-carboxylate (2) has been synthesized from ethyl naphtha [2,1-b]furan-2-carboxylate (1). This nitro product on reaction with hydrazine hydrate formed 3-nitronaphtho [2,1-b] furan-2-carbohydrazide (3). Various Schiff bases 3-nitro-N1(aryl-methylene)-substituted-naphtho [2,1-b]furan-2-carbohydrazides 4(a-g) were obtained by treating hydrazide (3) with different aldehydes. These Schiff bases on reaction with chloro acetyl chloride in presence of triethylamine in dioxane yielded 3-nitro-N-(3-chloro-2-oxo-substituted-phenyl-azetidine-1-yl) naphtha [2,1-b]furan-2-carboxamides 5(a-g). All the newly synthesized compounds have been characterized by spectral and analytical studies. The Schiff bases, 4a-g and azetidione derivatives, 5a-g have been studied for antioxidant and antimicrobial activities.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 0973-4945
2090-9810
Relation: https://doaj.org/toc/0973-4945; https://doaj.org/toc/2090-9810
DOI: 10.1155/2010/863547
URL الوصول: https://doaj.org/article/362ee8653f57423ea48bad114ffe8beb
رقم الأكسشن: edsdoj.362ee8653f57423ea48bad114ffe8beb
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:09734945
20909810
DOI:10.1155/2010/863547