dc.creatorNegri, G
dc.creatorKascheres, C
dc.date2001
dc.dateJAN-FEB
dc.date2014-07-31T14:19:00Z
dc.date2015-11-26T16:36:29Z
dc.date2014-07-31T14:19:00Z
dc.date2015-11-26T16:36:29Z
dc.date.accessioned2018-03-28T23:19:14Z
dc.date.available2018-03-28T23:19:14Z
dc.identifierJournal Of Heterocyclic Chemistry. Hetero Corporation, v. 38, n. 1, n. 109, n. 123, 2001.
dc.identifier0022-152X
dc.identifierWOS:000167547400016
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/75349
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/75349
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1271832
dc.descriptionThe reactions of 4-(methylamino)-3-penten-2-one with diazoketones yielded the alpha -acylenaminoketones 1-3 in good yields. Preparation of the alpha -acylenaminoketone 4 was carried out by treatment of 4-(t-butylamino)-3-penten-2-one with benzoyl chloride being followed by reaction of transamination with methylamine. The reactions were carried out in five different solvents land were submitted to gas chromatography/mass spectrometry analysis, with the goal of obtaining substituted pyrazoles and determining which of the carbonyls would preferentially be attacked by the nucleophile. The reactions of compounds 1-4 with hydrazine reagents led to the formation of the pyrazoles 5-7a-q. Small amounts of 4-methylamino-2-pentenones 10a-q, amides 11a-q and pyrazoles 12a-q were also obtained in these reactions. The unexpected formation of pyrazoles 15d,h,q was detected when methanol and N,N-dimethylformamide were used as solvents in the reactions of alpha -acylenaminoketone 4 with hydrazine reagents.
dc.description38
dc.description1
dc.description109
dc.description123
dc.languageen
dc.publisherHetero Corporation
dc.publisherOdessa
dc.publisherEUA
dc.relationJournal Of Heterocyclic Chemistry
dc.relationJ. Heterocycl. Chem.
dc.rightsfechado
dc.sourceWeb of Science
dc.subjectVersatile Synthesis
dc.subjectGrignard-reagents
dc.subjectCrystal-structure
dc.subjectEnaminones
dc.subjectDerivatives
dc.subjectAm1
dc.subjectK-10/ultrasound
dc.subjectPyrazolinones
dc.subjectAnnulation
dc.subjectKetones
dc.titleStudy of the reactivity of alpha-acylenaminoketones. Synthesis of pyrazoles
dc.typeArtículos de revistas


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