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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Madhusudhan, G | - |
| dc.contributor.author | Kumar, B Anand | - |
| dc.contributor.author | Chintamani, U S | - |
| dc.contributor.author | Rao, M Narasimha | - |
| dc.contributor.author | Udaykiran, D | - |
| dc.contributor.author | Suresh, T | - |
| dc.contributor.author | Kumar, V Kiran | - |
| dc.contributor.author | Mukkanti, K | - |
| dc.date.accessioned | 2010-05-04T10:43:36Z | - |
| dc.date.available | 2010-05-04T10:43:36Z | - |
| dc.date.issued | 2010-05 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/8755 | - |
| dc.description | 606-610 | en_US |
| dc.description.abstract | A facile synthesis of Carvedilol via a key 5-substituted-2-oxazolidinone intermediate is described and this approach avoids the formation of bis side product (impurity B). This approach could be useful for the preparation of many β-amino alcohols without formation of bis impurity. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | CSIR | en_US |
| dc.source | IJC-B Vol.49B(05) [May 2010] | en_US |
| dc.subject | Carvedilol | en_US |
| dc.subject | 5-substituted-2-oxazolidinone | en_US |
| dc.subject | impurity B | en_US |
| dc.subject | β-adrenergic blocking agent | en_US |
| dc.subject | β-amino alcohol | en_US |
| dc.title | A facile synthesis of carvedilol, β-adrenergic blocking agent, via a key 5-substituted-2-oxazolidinone intermediate | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.49B(05) [May 2010] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 49B(5) 606-610.pdf | 149.2 kB | Adobe PDF | View/Open |
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