Studies on quinones. Part 33. Synthetic approach to podands containing quinone fragments

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dc.contributor.authorValderrama, JA
dc.contributor.authorLeiva, H
dc.contributor.authorTapia, R
dc.date.accessioned2025-01-21T01:31:42Z
dc.date.available2025-01-21T01:31:42Z
dc.date.issued2000
dc.description.abstractThe preparation and oxidative demethylation attempts of podands 3-5, and 9 containing the 2,5-dimethoxyphenyl substituent are described. The reaction of alizarine 13 with chloroethanol afforded compounds 14 and 15. The pathway formation of heterocycle 15 from 14 is proposed. The synthesis of podand 16 containing the cytotoxic 1-hydroxy-9,10-anthraquinone fragment as the terminal groups is reported.
dc.fuente.origenWOS
dc.identifier.issn0039-7911
dc.identifier.urihttps://repositorio.uc.cl/handle/11534/97123
dc.identifier.wosidWOS:000085697300018
dc.issue.numero4
dc.language.isoen
dc.pagina.final749
dc.pagina.inicio737
dc.revistaSynthetic communications
dc.rightsacceso restringido
dc.titleStudies on quinones. Part 33. Synthetic approach to podands containing quinone fragments
dc.typeartículo
dc.volumen30
sipa.indexWOS
sipa.trazabilidadWOS;2025-01-12
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