Novel Fluorinated Spiro [Indole-indazolyl-thiazolidine]-2,4′-diones: Design and Synthesis

dc.contributor.authorSakhuja, Rajeev
dc.date.accessioned2021-11-11T11:02:39Z
dc.date.available2021-11-11T11:02:39Z
dc.date.issued2004-09-07
dc.description.abstractThe 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.identifier.urihttps://www.tandfonline.com/doi/abs/10.1080/104265090889431
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3397
dc.language.isoenen_US
dc.publisherTaylor & Francisen_US
dc.subjectChemistryen_US
dc.subjectFluorinated Spiroen_US
dc.subjectSynthesisen_US
dc.subjectMolecular modificationen_US
dc.titleNovel Fluorinated Spiro [Indole-indazolyl-thiazolidine]-2,4′-diones: Design and Synthesisen_US
dc.typeArticleen_US

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