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http://nopr.niscpr.res.in/handle/123456789/16314Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Dengle, R V | - |
| dc.contributor.author | Ingle, R D | - |
| dc.contributor.author | Bondge, S P | - |
| dc.contributor.author | Mane, R A | - |
| dc.date.accessioned | 2013-03-09T11:01:08Z | - |
| dc.date.available | 2013-03-09T11:01:08Z | - |
| dc.date.issued | 1999-03 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/16314 | - |
| dc.description | 390-393 | en_US |
| dc.description.abstract | 5-Acyl-2-aryl-4-methyl thiazoles 1 have been converted to 1-(2' -aryl-4' -methylthiazol-5' -yl)-3-aryl-2-propen-1-ones 2 by Claisen-Schmidt condensation. The chalcones 2 are brominated to give their bromo derivatives 3 which on hydrolysis yield 1-(2'aryl- 4' -methylthiazol-5'-yl)-3-arylpropane-1,3-diones 4. The diones 4 when condensed with 2-aminobenzenethiol in refluxing DMSO furnish cyclic product, 2-aroyl-3-(2'-aryl-4'methylthiazol- 5' -yl)-4H-1,4-benzothiazines 5. The results of microbial screening of the compounds 5 have been discussed. | 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(03) [March 1999] | en_US |
| dc.title | Synthesis and microbial activity of new thiazolyl 1,4-benzothiazines | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.38B(03) [March 1999] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 38B(3) 390-393.pdf | 765.91 kB | Adobe PDF | View/Open |
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