1987
DOI: 10.1002/chin.198736175
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ChemInform Abstract: Synthesis and Anticonvulsive Activity of 1‐R‐3‐Acetonyl‐3‐hydroxy Oxindole Oximes and Their Derivatives.

Abstract: 175ChemInform Abstract Oximes such as (I) are prepared by common methods and tested for their anticonvulsive effect. Compound (Ia) is the most active one.

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“…These compounds are also obtained in aldolic and related condensations with acetone 394 or its oxime 395 ; aromatic 396,397 and heteroaromatic methylketones 398,399 ; cyclic alkylketones 400 ; acetates 401 ; propionates 402 ; acetoacetates 403 ; cyanoacetates 404 ; nitroalkanes 405 ; benzodiazepinones 406 ; imidazolinones 407 ; indoles 408 ; 2-methylquinolines 409 ; pyrazinones 410 ; thiazolidinediones [411][412][413][414][415] and xanthinones 416 In the reaction of isatins with some cyclic ketones, such as 4-hydroxy-2H-benzopyran-2-one 417 , the initial dioxindole formed reacts with a second equivalent of the ketone yielding a 3,3-disubstituted oxindole.…”
Section: Scheme 96mentioning
confidence: 99%
“…These compounds are also obtained in aldolic and related condensations with acetone 394 or its oxime 395 ; aromatic 396,397 and heteroaromatic methylketones 398,399 ; cyclic alkylketones 400 ; acetates 401 ; propionates 402 ; acetoacetates 403 ; cyanoacetates 404 ; nitroalkanes 405 ; benzodiazepinones 406 ; imidazolinones 407 ; indoles 408 ; 2-methylquinolines 409 ; pyrazinones 410 ; thiazolidinediones [411][412][413][414][415] and xanthinones 416 In the reaction of isatins with some cyclic ketones, such as 4-hydroxy-2H-benzopyran-2-one 417 , the initial dioxindole formed reacts with a second equivalent of the ketone yielding a 3,3-disubstituted oxindole.…”
Section: Scheme 96mentioning
confidence: 99%