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http://nopr.niscpr.res.in/handle/123456789/751Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Solankee, Anjani | - |
| dc.contributor.author | Kapadia, Kishor | - |
| dc.contributor.author | Solankee, Pankit | - |
| dc.contributor.author | Prajapati, Yogesh | - |
| dc.contributor.author | Patel, Hiral | - |
| dc.contributor.author | Solankee, Sejal | - |
| dc.date.accessioned | 2008-04-04T10:50:03Z | - |
| dc.date.available | 2008-04-04T10:50:03Z | - |
| dc.date.issued | 2007-10 | - |
| dc.identifier.issn | 0376-4699 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/751 | - |
| dc.description | 1707-1712 | en_US |
| dc.description.abstract | An elegant synthesis of the titled compounds 7a-e, 8a-e and 9a-e have been presented starting from chalcones 6a-e based on s-triazine nucleus. These chalcones 6a-e on cyclisation with guanidine nitrate and hydroxylamine hydrochloride in the presence of alkali give aminopyrimidines 7a-e and isoxazoles 8a-e respectively. Further these chalcones 6a-e on cyclisation with 2-aminothiophenol in the presence of few drops of glacial acetic acid give 1,5-benzothiazepines 9a-e. All the products obtained from these reactions are characterized by elemental analysis, IR, ¹H NMR and mass spectral data. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | CSIR | en_US |
| dc.source | IJCB Vol.46B(10) [October 2007] | en_US |
| dc.subject | Aminopyrimidines | en_US |
| dc.subject | Isoxazoles | en_US |
| dc.subject | 1,5-benzothiazepines | en_US |
| dc.subject | Glacial acetic acid | en_US |
| dc.subject | Chalcones | en_US |
| dc.subject | s-triazine nucleus | en_US |
| dc.title | Synthesis and studies of some novel s-triazine based aminopyrimidines, isoxazoles and 1,5-benzothiazepines | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.46B(10) [October 2007] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 46B(10) (2007) 1707-1712.pdf | 108.25 kB | Adobe PDF | View/Open |
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