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http://nopr.niscpr.res.in/handle/123456789/8941Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Madhusudhan, G | - |
| dc.contributor.author | Reddy, G Om | - |
| dc.contributor.author | Ramanatham, J | - |
| dc.contributor.author | Dubey, P K | - |
| dc.date.accessioned | 2010-05-14T11:15:49Z | - |
| dc.date.available | 2010-05-14T11:15:49Z | - |
| dc.date.issued | 2005-02 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/8941 | - |
| dc.description | 366-371 | en_US |
| dc.description.abstract | Novel syn-N-arylsulfonyl-4-substituted
phenyl-2-oxo-1,3-oxazolidine-5-carboxylates have been synthesized from the
corresponding -azido alcohols and converted to their anti-form
by epimerizing C-2 proton using DBU. Studies on the stabilization energies are
done to evaluate conversion from syn-to anti-and not the
vice-versa. All the compounds have been tested for their in vitro anti-bacterial
activity against S. aureus, E. faecalis and E. faecium. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | CSIR | en_US |
| dc.relation.ispartofseries | Int.Cl.7 C 07 D 263/00 // A 61 P 31/04 | en_US |
| dc.source | IJC-B Vol.44B(02) [February 2005] | en_US |
| dc.title | Synthesis of syn-N-aryl sulfonyl-4-substituted phenyl-2-oxo-1,3-oxazolidine-5-carboxylates and their conversion to ant-form using DBU | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.44B(02) [February 2005] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 44B(2) 366-371.pdf | 119.51 kB | Adobe PDF | View/Open |
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-azido alcohols and converted to their anti-form
by epimerizing C-2 proton using DBU. Studies on the stabilization energies are
done to evaluate conversion from syn-to anti-and not the
vice-versa. All the compounds have been tested for their in vitro anti-bacterial
activity against S. aureus, E. faecalis and E. faecium.