dc.contributor.author
Vicente García, Esther
dc.contributor.author
Ramón, Rosario
dc.contributor.author
Preciado Gallego, Sara
dc.contributor.author
Lavilla Grífols, Rodolfo
dc.date.issued
2018-03-08T14:32:18Z
dc.date.issued
2018-03-08T14:32:18Z
dc.date.issued
2018-03-08T14:32:18Z
dc.identifier
https://hdl.handle.net/2445/120564
dc.description.abstract
The tetrahydroquinolines obtained through the Povarov multicomponent reaction have been oxidized to the corresponding quinoline, giving access to a single product through a two-step sequence. Several oxidizing agents were studied and manganese dioxide proved to be the reagent of choice, affording higher yields, cleaner reactions and practical protocols.
dc.format
application/pdf
dc.publisher
Beilstein Institute
dc.relation
Reproducció del document publicat a: https://doi.org/10.3762/bjoc.7.110
dc.relation
Beilstein Journal of Organic Chemistry, 2011, vol. 7, p. 980-987
dc.relation
https://doi.org/10.3762/bjoc.7.110
dc.rights
cc-by (c) Vicente García, Esther et al., 2011
dc.rights
http://creativecommons.org/licenses/by/3.0/es
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)
dc.subject
Síntesi orgànica
dc.subject
Organic synthesis
dc.title
Multicomponent reaction access to complex quinolines via oxidation of the povarov adducts
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion
