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http://nopr.niscpr.res.in/handle/123456789/9719Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Mogilaiah, K | - |
| dc.contributor.author | Kumar, K Shiva | - |
| dc.contributor.author | Swamy, J Kumara | - |
| dc.contributor.author | Chandra, A Vinay | - |
| dc.date.accessioned | 2010-06-08T05:43:52Z | - |
| dc.date.available | 2010-06-08T05:43:52Z | - |
| dc.date.issued | 2010-06 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/9719 | - |
| dc.description | 840-844 | en_US |
| dc.description.abstract | A simple and highly efficient procedure has been described for the synthesis of 1-(5-aryl-[1,3,4]-oxadiazol-2-ylmethyl)-3-(3-methylphenyl)-1H-[1,8]naphthyridin-2-ones 5 by the oxidation of the corresponding [2-oxo-3-(3-methylphenyl)-2H-[1,8]naphthyridin-1-yl]acetic acid arylidenehydrazides 4 with iodobenzene diacetate [ PhI(OAc)2] in solid state. The products are obtained in good yields and in a state of high purity. The structural assignments of compounds 2-5 are based on their elemental analyses and spectral (IR and 1 H NMR) data. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | CSIR | en_US |
| dc.source | IJC-B Vol.49B(06) [June 2010] | en_US |
| dc.subject | 1,3,4-Oxadiazoles | en_US |
| dc.subject | 1,8-naphthyridines | en_US |
| dc.subject | iodobenzene diacetate [ PhI(OAc)2] | en_US |
| dc.subject | solid state | en_US |
| dc.title | Efficient synthesis of 1,3,4-oxadiazolyl-1,8-naphthyridines using iodobenzene diacetate in solid state | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.49B(06) [June 2010] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 49B(6) 840-844.pdf | 86.42 kB | Adobe PDF | View/Open |
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