REACTION OF TETRAHYDROBENZ[A]ACRIDINONES WITH HYDROXYLAMINE HYDROCHLORIDE .7.

dc.contributor.author	RUBIO, MF
dc.contributor.author	CAMACHO, T
dc.contributor.author	LINZAGA, I
dc.contributor.author	MANCERA, C
dc.contributor.author	Martínez, R
dc.contributor.author	Ramirez, G
dc.date.accessioned	2011-01-22T10:28:28Z
dc.date.available	2011-01-22T10:28:28Z
dc.date.issued	1995
dc.identifier.issn	0022-152X
dc.identifier.uri	http://hdl.handle.net/11154/3423
dc.description.abstract	Oximation of ortho-substituted phenylbenz[a]acridinones using hydroxylamine hydrochloride, sodium hydroxide and ethanol as the solvent gave always the benzoquinacridine N-oxide 2. Oximation of parasubstituted phenylbenz[a]acridinones, however, gave only the corresponding oximes. The structure of all products was corroborated by ir, H-1 and C-13-nmr and mass spectral data. Theoretical calculations support the experimental findings.	en_US
dc.language.iso	en	en_US
dc.title	REACTION OF TETRAHYDROBENZ[A]ACRIDINONES WITH HYDROXYLAMINE HYDROCHLORIDE .7.	en_US
dc.type	Article	en_US
dc.identifier.idprometeo	3171
dc.source.novolpages	32(3):827-830
dc.subject.wos	Chemistry, Organic
dc.description.index	WoS: SCI, SSCI o AHCI
dc.relation.journal	Journal of Heterocyclic Chemistry