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

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DC Field	Value	Language
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
Appears in Collections:	Department of Chemistry

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