Site selectivity in the reaction of 2-formyl-2H-azirine-N-arylimines with diphenylketene

dc.creatorJunior, JN
dc.creatorKascheres, A
dc.date1997
dc.dateJAN-FEB
dc.date2014-12-16T11:37:19Z
dc.date2015-11-26T17:27:40Z
dc.date2014-12-16T11:37:19Z
dc.date2015-11-26T17:27:40Z
dc.date.accessioned2018-03-29T00:14:48Z
dc.date.available2018-03-29T00:14:48Z
dc.identifierJournal Of Heterocyclic Chemistry. Hetero Corporation, v. 34, n. 1, n. 341, n. 343, 1997.
dc.identifier0022-152X
dc.identifierWOS:A1997WM42900054
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/74303
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/74303
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/74303
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1284855
dc.description2-Formyl-2H-azirine-N-arylimines lac react with diphenylketene 2 to afford 2H-2-azirinyl-2-azetidinones 3a-c and N-aryldiphenylacetamides 4a-c by reaction at the exo-imine group. Derivatives containing the bulkier methyl group at the 2-position, 1d-f, produce only 4a-c.
dc.description34
dc.description1
dc.description341
dc.description343
dc.languageen
dc.publisherHetero Corporation
dc.publisherOdessa
dc.relationJournal Of Heterocyclic Chemistry
dc.relationJ. Heterocycl. Chem.
dc.rightsfechado
dc.sourceWeb of Science
dc.titleSite selectivity in the reaction of 2-formyl-2H-azirine-N-arylimines with diphenylketene
dc.typeArtículos de revistas


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