{"id":56885,"date":"2007-02-02T00:00:00","date_gmt":"2007-02-02T00:00:00","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/reacciones-electroqua%c2%admicas-pareadas-y-otros-procesos-electrosinteticos-de-interes\/"},"modified":"2007-02-02T00:00:00","modified_gmt":"2007-02-02T00:00:00","slug":"reacciones-electroqua%c2%admicas-pareadas-y-otros-procesos-electrosinteticos-de-interes","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/mecanismos-de-las-reacciones-organicas\/reacciones-electroqua%c2%admicas-pareadas-y-otros-procesos-electrosinteticos-de-interes\/","title":{"rendered":"Reacciones electroqu\u00edmicas pareadas y otros procesos electrosint\u00e9ticos de inter\u00e9s"},"content":{"rendered":"<h2>Tesis doctoral de <strong> Mar\u00eda Dolores Otero Del R\u00edo <\/strong><\/h2>\n<p>2,4,6-trimetilpiridina-3,5-dicarbonitrilo se obtuvo como producto mayoritario despu\u00e9s de realizar la electr\u00f3lisis de acetonitrilo en presencia de bisulfato de tetrabutilamonio como electrolito soporte, utilizando una c\u00e9lula con separaci\u00f3n de compartimentos mediante un diafragma de vidrio fritado de 3,4,5-tricarbonitrilo en menor proporci\u00f3n. se realiz\u00f3 una primera aproximaci\u00f3n en la utilizaci\u00f3n del co2 ani\u00f3n radical para la transformaci\u00f3n de propionitrilo y butironitrilo en \u00e1cidos alfa-metil y alfa-atilcianoac\u00e9ticos a trav\u00e9s de una reacci\u00f3n electroqu\u00edmica pareada con co2. Tambi\u00e9n se discute la electros\u00edntesis del \u00e1cido alfa-clorofenilac\u00e9tico a partir de cloruro de bencilo y del \u00e1cido fenilac\u00e9tico a partir de tolueno. la electr\u00f3lisis de tetrafloroboratos de arildiazonio en dmf seco y bu4nhso4 como disolvente-electrolito soporte, en presencia de co2 da lugar a la formaci\u00f3n de los correspondientes \u00e1cidos arilcarbox\u00edlicos con buenos rendimientos.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Reacciones electroqu\u00edmicas pareadas y otros procesos electrosint\u00e9ticos de inter\u00e9s<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Reacciones electroqu\u00edmicas pareadas y otros procesos electrosint\u00e9ticos de inter\u00e9s <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Mar\u00eda Dolores Otero Del R\u00edo <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Alcal\u00e1<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 02\/02\/2007<\/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>Fructuoso Barba Valiente<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Antonio Aldaz riera <\/li>\n<li>isidoro Barba merino (vocal)<\/li>\n<li>toribio Fernandez otero (vocal)<\/li>\n<li>Francisco Vicente pedr\u00f3s (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Mar\u00eda Dolores Otero Del R\u00edo 2,4,6-trimetilpiridina-3,5-dicarbonitrilo se obtuvo como producto mayoritario despu\u00e9s de realizar la electr\u00f3lisis de [&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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