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Please use this identifier to cite or link to this item: http://hdl.handle.net/11154/3423

Title: REACTION OF TETRAHYDROBENZ[A]ACRIDINONES WITH HYDROXYLAMINE HYDROCHLORIDE .7.
Authors: RUBIO, MF
CAMACHO, T
LINZAGA, I
MANCERA, C
Martínez, R
Ramirez, G
Issue Date: 1995
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.
URI: http://hdl.handle.net/11154/3423
ISSN: 0022-152X
Appears in Collections:Ciencias

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