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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kidwai, Mazaahir | - |
| dc.contributor.author | Kumar, Rajesh | - |
| dc.contributor.author | Kohli, Seema | - |
| dc.date.accessioned | 2013-03-29T14:45:14Z | - |
| dc.date.available | 2013-03-29T14:45:14Z | - |
| dc.date.issued | 1999-09 | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/16611 | - |
| dc.description | 1132-1135 | en_US |
| dc.description.abstract | N,N-Bis (2-hydroxyethyl) amino substituted propiophenones 2a-c have been prepared using Mannich reaction from substituted acetophenones 1a-c. 2a-c on hydrazinolysis yield 3a-f which on chlorination give nitrogen mustards 4a-f. 4a-f on reaction with chloracetyl chloride, N-methylmorpholine and chlorobenzene under mircrowave activation (MWI) afford β-lactams 5a-f while cyclisation of 4a-f with polyphosphoric acid under MWI give the indoles 6a-f. | 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(09) [September 1999] | en_US |
| dc.title | Microwave-induced synthesis of nitrogen-mustard derivatives | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.38B(09) [September 1999] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 38B(9) 1132-1135.pdf | 716.55 kB | Adobe PDF | View/Open |
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