Please use this identifier to cite or link to this item:
http://nopr.niscpr.res.in/handle/123456789/16516Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Subramanian, G B V | - |
| dc.contributor.author | Sen, Somdutta | - |
| dc.date.accessioned | 2013-03-27T20:03:04Z | - |
| dc.date.available | 2013-03-27T20:03:04Z | - |
| dc.date.issued | 1999-07 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/16516 | - |
| dc.description | 854-856 | en_US |
| dc.description.abstract | ω-Chloro, bromo and iodo compounds with one carbon less have been obtained from aleuritic acid and its derivatives as potential synthetic intermediates using N-hydroxypyridine-2-thione (Barton's procedure). | 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(07) [July 1999] | en_US |
| dc.title | Decarboxylative-halogenation of aleuritic acid and its derivatives using N-hydroxypyridine- 2-thione and a halogen source | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.38B(07) [July 1999] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 38B(7) 854-856.pdf | 568.2 kB | Adobe PDF | View/Open |
Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.