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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Majo, V J | - |
| dc.contributor.author | Anand, R Vijaya | - |
| dc.contributor.author | Perumal, P T | - |
| dc.date.accessioned | 2013-03-27T19:51:01Z | - |
| dc.date.available | 2013-03-27T19:51:01Z | - |
| dc.date.issued | 1999-07 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/16508 | - |
| dc.description | 763-765 | en_US |
| dc.description.abstract | An attempted synthesis of oxazolium salts from 1-aryl-2- (arylamino)ethanones under VilsmeiEr conditions results in the formation of 1-aryl-2-(N-formyl-N-arylamino)ethanones 4 as the major product. Vinyl chlorides are obtained in low yield by the reaction of carbonyl group only in a few cases. The proposed reaction mechanism involves the formation of an intermediate cyclic oxazolidine derivative which accounts for the low reactivity of carbonyl group and lack of formation of N-formylvinyl chloride. | 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 | The unusual behaviour of substituted 1-aryl-2-(arylamino)ethanones towards Vilsmeier reagent | 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) 763-765.pdf | 616.95 kB | Adobe PDF | View/Open |
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