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- W2064444804 abstract "7-Methyloctahydroacridines 7a–d were obtained by a one-pot imine condensation/Lewis acid-catalyzed cyclization from aniline derivatives 5a–d and aldehyde 6. Only those compounds 7 could be oxidized with DDQ to the corresponding octahydroacridine-7-carbaldehydes 9, which bear a meta-chloro or bromo substituent (with respect to the methyl group) in addition to the para-amino group (i.e. 7c,d → 9c,d). Aldehyde 9c was further converted to the novel tripodand 11 which was characterized by X-ray crystal structure analysis." @default.
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- W2064444804 date "1998-01-01" @default.
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- W2064444804 title "Convenient preparation of aromatic aldehydesvia DDQ oxidation. Application in the Synthesis of a Tripodand Containing Octahydroacridine Moieties" @default.
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- W2064444804 doi "https://doi.org/10.1002/prac.19983400408" @default.
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