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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Reddy, C Devendranath | - |
| dc.contributor.author | Reddy, M S | - |
| dc.contributor.author | Raju, C Naga | - |
| dc.date.accessioned | 2013-03-31T13:31:35Z | - |
| dc.date.available | 2013-03-31T13:31:35Z | - |
| dc.date.issued | 2000-06 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/16708 | - |
| dc.description | 426-432 | en_US |
| dc.description.abstract | Synthesis of 2-aryloxy/alkyl/phenyl-6-methyl-4H-1,3,2-dioxaphosphorino[5,4-b]- pyridine-2-oxides has been accomplished by condensation of equimolar quantities of various substituted phenylphosphorodichloridates and alkylphosphonic dichlorides with 3-hydroxy-6-methyl-2-pyridine-methanol (lutidine diol) in the presence of triethylamine in dry benzenepyridine. Their structures have been established by elemental analysis, IR, NMR (1H,13C and 31P) and mass spectral data. A few compounds have been screened for their expected antibacterial and antifungal activities.All the compounds exhibit molecular ions with high abundance and (M-OAr)+ ions are the base peaks in their mass spectra. Long range C-P coupling constant values are evaluated. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights |  CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJC-B Vol.39B(06) [June 2000] | en_US |
| dc.title | Synthesis, NMR (1H, 13C and 31P), mass spectral studies and biological activity of 2-aryloxy/alkyl-6-methyl- 1,3,2-dioxaphosphorino[5,4-b]pyridine-2-oxides | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.39B(06) [June 2000] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 39B(6) 426-432.pdf | 1.26 MB | Adobe PDF | View/Open |
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