Synthesis of 2-hydroxy-3-substituted naphthoquinones using the Heck reaction

dc.creatorPérez Sánchez, Alice Lorena
dc.creatorLamoureux Lamontagne, Guy
dc.creatorZhen-Wu, Bi Yun
dc.date.accessioned2016-07-28T20:34:04Z
dc.date.accessioned2019-04-25T14:33:17Z
dc.date.available2016-07-28T20:34:04Z
dc.date.available2019-04-25T14:33:17Z
dc.date.created2016-07-28T20:34:04Z
dc.date.issued2007-06
dc.identifierhttp://www.sciencedirect.com/science/article/pii/S0040403907006922
dc.identifier0040-4039
dc.identifierhttp://hdl.handle.net/10669/28843
dc.identifier10.1016/j.tetlet.2007.04.033
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/2371549
dc.description.abstractAn efficient Heck coupling of 2-hydroxy-3-iodo-naphthoquinone with a series of electron-deficient alkenes in aqueous solution has been accomplished. The method is characterized by simple conditions and facile work-up to isolate the products in good to excellent yields. The products contain the motif present in several naphthoquinone pigments but with enhanced polarity.
dc.languageen_US
dc.sourceTetrahedron Letters 48(23): 3995–3998, 4 Junio 2007
dc.subjectHeck reaction
dc.subjectHooker condensation
dc.subjectNaphthoquinone
dc.subject2-Hydroxy-3-iodonaphthoquinone
dc.titleSynthesis of 2-hydroxy-3-substituted naphthoquinones using the Heck reaction
dc.typeArtículos de revistas
dc.typeArtículo científico


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