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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Pandey, V K | - |
| dc.contributor.author | Pathak, Seema R | - |
| dc.date.accessioned | 2013-03-29T14:40:16Z | - |
| dc.date.available | 2013-03-29T14:40:16Z | - |
| dc.date.issued | 1999-09 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/16608 | - |
| dc.description | 1111-1113 | en_US |
| dc.description.abstract | 7-Hydroxy-4-methylcoumarin 1 on treatment with p-phenylenediamine gives 1-(p-aminophenyl)-4-methyl-7-hydroxy-carbostyril 2 which reacts with aromatic aldehydes affording 1-(p-arylidenophenyl)-4-methyl-7-hydroxycarbostyril 3. Interaction of 3 with aromatic amine in presence of anhyd. ZnCI2 results in the formation of 1-(p-arylidenophenyl)-4-methyl-7-arylaminocarbostyril 4 which undergoes cyclisation with sulphur and iodine giving 1-(p-arylidenophenyl )-2-oxo-4-methylpyrido[b]phenothia-zines 5. The antidiabetic and antiviral activities of 5 have been reported. | 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.38B(09) [September 1999] | en_US |
| dc.title | Synthesis of 1-(p-arylldenophenyl)-2-oxo-4-methylpyrido[b]phenothiazines | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.38B(09) [September 1999] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 38B(9) 1111-1113.pdf | 615.82 kB | Adobe PDF | View/Open |
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