Design and synthesis of angucyclinone 5-aza analogues

dc.creatorValderrama, Jaime A.
dc.creatorGonzalez, M. Florencia
dc.creatorColonelli, Pamela
dc.creatorVasquez, David
dc.date.accessioned2024-01-10T12:04:52Z
dc.date.available2024-01-10T12:04:52Z
dc.date.created2024-01-10T12:04:52Z
dc.date.issued2006
dc.identifier10.1055/s-2006-950254
dc.identifier1437-2096
dc.identifier0936-5214
dc.identifierhttps://doi.org/10.1055/s-2006-950254
dc.identifierhttps://repositorio.uc.cl/handle/11534/75898
dc.identifierWOS:000242059100018
dc.description.abstractA highly efficient one-pot procedure for the synthesis of phenanthridine-1,7,10-triones from acylbenzoquinones and cyclic enaminones is reported. The cycloaddition reactions of these quinones with 1-trimethylsilyloxybutadiene followed by hydrolysis and oxidative processes provide entry to a variety of angucyclinone 5-aza analogues.
dc.languageen
dc.publisherGEORG THIEME VERLAG KG
dc.rightsacceso restringido
dc.subjectMichael additions
dc.subjectquinones
dc.subjectheterocycles
dc.subjectDiels-Alder reactions
dc.subjectregioselectivity
dc.subjectDIELS-ALDER REACTION
dc.subjectQUINONES
dc.subjectCYTOTOXICITY
dc.subjectHYDROQUINONES
dc.subjectBENZOQUINONES
dc.subjectANTIBIOTICS
dc.subjectACCESS
dc.subjectRING
dc.titleDesign and synthesis of angucyclinone 5-aza analogues
dc.typeartículo


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