{"id":102139,"date":"2018-03-11T10:24:12","date_gmt":"2018-03-11T10:24:12","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/reactividad-de-iminas-con-organoboranos-aspectos-sinteticos-y-mecana%c2%adsticos\/"},"modified":"2018-03-11T10:24:12","modified_gmt":"2018-03-11T10:24:12","slug":"reactividad-de-iminas-con-organoboranos-aspectos-sinteticos-y-mecana%c2%adsticos","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/organometalicos\/reactividad-de-iminas-con-organoboranos-aspectos-sinteticos-y-mecana%c2%adsticos\/","title":{"rendered":"Reactividad de iminas con organoboranos: aspectos sint\u00e9ticos y mecan\u00edsticos"},"content":{"rendered":"<h2>Tesis doctoral de <strong> Mar\u00eda  Carmen Mu\u00f1oz Hernandez <\/strong><\/h2>\n<p>T\u00edtulo de la tesis: reactividad de iminas con organoboranos: aspectos sint\u00e9ticos y mecan\u00edsticos resumen: se ha. Estirado la reactividad de bisarilaldiminas con dialquilcloroboranos con restos alquilicos primarios y secundarios. Adem\u00e1s se ha desarrollado un proceso one-pot que envuelve tres componentes: derivados del benzaldeh\u00eddo, aril iminas y dialquilcloroboranos como agente alquilante. En todos los casos se han obtenido las correspondientes aminas en muy buenos rendimientos. Este mismo proceso one-pot se ha puesto a punto para la obtenci\u00f3n de aminas utilizando trialquilboranos. Se han estudiado una serie de trialquilbqranos con restos alquilicos primarios y secundarios as\u00ed como diferentes aldehidos arom\u00e1ticos con distintos sustituyentes dadores y aceptores d\u00e9 electrones* siendo en todos los casos los rendimientos de muy buenos a excelentes. : este m\u00e9todo de alquilaci\u00f3n se ha aplicado sobre iminas enolizables o iminas .Iv-alqu\u00edlicas. Los buenos resultados obtenidos confirman la versatilidad de la reacci\u00f3n. se ha realizado un estudio sobre iminas quirales, donde la quiralidad es aportada por el resto del aldehido o de la amina. As\u00ed, se han conseguido sintetizar eficientemente una serie de aminas quirales con excelentes rendimientos y buenas relaciones diasteroisom\u00e9ricas.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Reactividad de iminas con organoboranos: aspectos sint\u00e9ticos y mecan\u00edsticos<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Reactividad de iminas con organoboranos: aspectos sint\u00e9ticos y mecan\u00edsticos <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Mar\u00eda  Carmen Mu\u00f1oz Hernandez <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 M\u00e1laga<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 28\/06\/2010<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n<h3>Direcci\u00f3n y tribunal<\/h3>\n<ul>\n<li><strong>Director de la tesis<\/strong>\n<ul>\n<li>Rafael Suau Suarez<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Luis Castedo exposito <\/li>\n<li>esther Lete exposito (vocal)<\/li>\n<li>christina Despotopoulou (vocal)<\/li>\n<li>Jos\u00e9 Fuentes mota (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Mar\u00eda Carmen Mu\u00f1oz Hernandez T\u00edtulo de la tesis: reactividad de iminas con organoboranos: aspectos sint\u00e9ticos y mecan\u00edsticos [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"site-sidebar-layout":"default","site-content-layout":"","ast-site-content-layout":"","site-content-style":"default","site-sidebar-style":"default","ast-global-header-display":"","ast-banner-title-visibility":"","ast-main-header-display":"","ast-hfb-above-header-display":"","ast-hfb-below-header-display":"","ast-hfb-mobile-header-display":"","site-post-title":"","ast-breadcrumbs-content":"","ast-featured-img":"","footer-sml-layout":"","theme-transparent-header-meta":"","adv-header-id-meta":"","stick-header-meta":"","header-above-stick-meta":"","header-main-stick-meta":"","header-below-stick-meta":"","astra-migrate-meta-layouts":"default","ast-page-background-enabled":"default","ast-page-background-meta":{"desktop":{"background-color":"var(--ast-global-color-4)","background-image":"","background-repeat":"repeat","background-position":"center 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