| dc.contributor.author | Sakhuja, Rajeev | |
| dc.date.accessioned | 2021-11-11T11:02:39Z | |
| dc.date.available | 2021-11-11T11:02:39Z | |
| dc.date.issued | 2004-09-07 | |
| dc.identifier.uri | https://www.tandfonline.com/doi/abs/10.1080/104265090889431 | |
| dc.identifier.uri | http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3397 | |
| dc.description.abstract | The reaction of indol-2,3-diones ( 1a–i ) with 5-aminoindazole ( 2 ) has resulted in the formation of hitherto unknown 3-(indazol-5-yl)iminoindol-2-ones ( 3a–i ) in quantitative yields which, on 1,3-dipolar cyclocondensation with mercaptoacetic acid ( 4 ), has afforded a series of new spiro heterocycles, 3′-(indazol-5-yl) spiro[3H, indol-3, 2′ -thiazolidine]-2,4′-diones* ( 5a–i ). | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Taylor & Francis | en_US |
| dc.subject | Chemistry | en_US |
| dc.subject | Fluorinated Spiro | en_US |
| dc.subject | Synthesis | en_US |
| dc.subject | Molecular modification | en_US |
| dc.title | Novel Fluorinated Spiro [Indole-indazolyl-thiazolidine]-2,4′-diones: Design and Synthesis | en_US |
| dc.type | Article | en_US |
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