Please use this identifier to cite or link to this item:
http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/2919Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kumar, Anil | - |
| dc.date.accessioned | 2021-10-27T04:09:41Z | - |
| dc.date.available | 2021-10-27T04:09:41Z | - |
| dc.date.issued | 2012-09-10 | - |
| dc.identifier.uri | https://onlinelibrary.wiley.com/doi/abs/10.1002/jhet.904?jhet904-eo-0005= | - |
| dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2919 | - |
| dc.description.abstract | A novel and efficient one-pot procedure has been described for synthesis of 2,4-disubstituted thiazoles and oxazoles from substituted ketones using phenyltrimethylammoniumtribromide as in situ brominating agent followed by reaction with thioamide/thiourea and amides/ureas, respectively in [bmim][BF4] ionicliquid. The advantages of the procedure include avoiding the handling of lacrymetric compounds, hazardous and toxic organic solvents along with good to excellent yield of the products. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Wiley | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | Thiazoles | en_US |
| dc.subject | Oxazoles | en_US |
| dc.subject | Phenyltrimethylammoniumtribromide | en_US |
| dc.title | A Novel and Efficient One Pot Synthesis of 2,4-Disubstituted Thiazoles and Oxazoles Using Phenyltrimethylammoniumtribromide in Ionic Liquid | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | Department of Chemistry | |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.