Please use this identifier to cite or link to this item:
http://nopr.niscpr.res.in/handle/123456789/22501Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Sharma, S D | - |
| dc.contributor.author | Saluja, Aarti | - |
| dc.contributor.author | Bhaduri, Susmita | - |
| dc.date.accessioned | 2013-10-23T04:37:27Z | - |
| dc.date.available | 2013-10-23T04:37:27Z | - |
| dc.date.issued | 2000-02 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/22501 | - |
| dc.description | 156-159 | en_US |
| dc.description.abstract | β-Lactam ring has been conveniently grafted onto 2-phenyl-5,6-dihydro-1,3 -thiazine 1 by annelating it with in situ prepared ketenes to furnish cepham analogues 6-9. A variety of acids such as menthoxy acetic acid 2, butylthioacetic acid 3, chloroacetic acid 4 and benzotriazole acetic acid 5 have been used as mixed sulphonic acid anhydrides for the cycloaddition reaction. All the compounds have been screened for their antibacterial activities. | 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(02) [February 2000] | en_US |
| dc.title | Studies on fused β-lactams: Synthesis, stereochemistry and antimicrobial activity of some new cepham analogues | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.39B(02) [February 2000] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 39B(2) 156-159.pdf | 725.46 kB | Adobe PDF | View/Open |
Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.