Please use this identifier to cite or link to this item:
Full metadata record
DC FieldValueLanguage
dc.contributor.authorMogilaiah, K-
dc.contributor.authorVenkanna, Ch-
dc.contributor.authorRao, A Nageswara-
dc.contributor.authorBabu, H Ramesh-
dc.identifier.issn0975-0983(Online); 0376-4699(Print)-
dc.description.abstractAn efficient and mild method for the synthesis of 2-(2-substituted[1,8]naphthyridin-3-yl)-5-(substituted-2-thienyl)-1,3,4-oxadiazoles 4 is reported by the oxidation of the corresponding Nʹ3-[1-(substituted-2-thienyl)methylidene]-2-sustituted[1,8]naphthyridine-3-carbohydrazides 3 with iodobenzene diacetate(PhI(OAc)2] in solid state. The reaction proceeds efficiently giving the products in good yields and excellent purities. The structural assignments of compounds 3 and 4 are based on their elemental analyses andspectral (IR, 1H NMR and MS) data. The compounds 4 have been screened for their antibacterial and anti-inflammatory activities.en_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.56B(06) [June 2017]en_US
dc.subjectIodobenzene diacetate[ PhI(OAc)2] solid stateen_US
dc.subjectAntibacterial activityen_US
dc.subjectAnti-inflammatory activityen_US
dc.titleGreen synthesis, antibacterial and anti-inflammatory activities of 2-(2-substituted[1,8]naphthyridin-3-yl)-5-(substituted-2-thienyl)-1,3,4-oxadiazolesen_US
Appears in Collections:IJC-B Vol.56B(06) [June 2017]

Files in This Item:
File Description SizeFormat 
IJCB 56B(6) 670-676.pdf131.14 kBAdobe PDFView/Open

Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.