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dc.contributor.authorMORALES RIOS, MARTHA SONIA-
dc.contributor.authorRIVERA BECERRIL, ERNESTO-
dc.contributor.authorLOPEZ CAMACHO, PERLA YOLANDA-
dc.contributor.authorPEREZ ROJAS, NADIA-
dc.contributor.authorSUAREZ CASTILLO, OSCAR-
dc.coverage.spatial<dc:creator id="info:eu-repo/dai/mx/cvu/93">MARTHA SONIA MORALES RIOS</dc:creator>-
dc.coverage.spatial<dc:creator id="info:eu-repo/dai/mx/cvu/45058">ERNESTO RIVERA BECERRIL</dc:creator>-
dc.coverage.spatial<dc:creator id="info:eu-repo/dai/mx/cvu/227390">PERLA YOLANDA LOPEZ CAMACHO</dc:creator>-
dc.coverage.spatial<dc:creator id="info:eu-repo/dai/mx/cvu/18735">OSCAR RODOLFO SUAREZ CASTILLO</dc:creator>-
dc.coverage.temporal<dc:subject>info:eu-repo/classification/cti/2</dc:subject>-
dc.date.accessioned2020-04-07T22:14:10Z-
dc.date.available2020-04-07T22:14:10Z-
dc.date.issued2012-
dc.identifier.citationNatural product communications, vol. 7, núm. 11, 2012en_US
dc.identifier.urihttp://ilitia.cua.uam.mx:8080/jspui/handle/123456789/324-
dc.description.abstractA practical procedure for the preparation of O-methyl substituted 3a,8-dialkyl-2-oxofuroindolines is described. Reductive lactonization of the corresponding oxindol-3-ylacetic acids provides a route for the formation of this class of compounds. Further transformation of 2-oxofuroindolines into 2-oxopyrrolidinoindolines, and then to pyrrolidinoindolines demonstrates their versatility as key intermediates in natural products synthesis. The results of single-crystal X-ray crystallographic analyses are given for five of the studied compounds.en_US
dc.description.sponsorshipNatural product communicationsen_US
dc.language.isoInglésen_US
dc.publisherWesterville, USA : Natural products Inc.en_US
dc.relation.haspart1555-9475-
dc.rightshttps://journals.sagepub.com/doi/abs/10.1177/1934578X1200701110-
dc.rightshttps://doi.org/10.1177/1934578X1200701110-
dc.subjectFarmacología - Investigacionesen_US
dc.subjectQuímica farmaceútica - Análisisen_US
dc.subjectSíntesis (Química inorgánica)en_US
dc.titlePreparation of O-methyl substituted 2-oxofuro-and 2-oxopyrrolidinoindolines by reductive lactonization of oxindol-3-ylacetic acids.en_US
dc.typeArtículoen_US
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