{"id":59751,"date":"2007-06-07T00:00:00","date_gmt":"2007-06-07T00:00:00","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/n-aminidas-de-piridinio-en-reacciones-radicalarias\/"},"modified":"2007-06-07T00:00:00","modified_gmt":"2007-06-07T00:00:00","slug":"n-aminidas-de-piridinio-en-reacciones-radicalarias","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/radicales-libres\/n-aminidas-de-piridinio-en-reacciones-radicalarias\/","title":{"rendered":"N-aminidas de piridinio en reacciones radicalarias"},"content":{"rendered":"<h2>Tesis doctoral de <strong> Aranzazu Sanchez Mu\u00f1oz <\/strong><\/h2>\n<p>En el curso de nuestros estudios en la reactividad de las n-heteroarilaminidas de pirdinio se ha desarrollo un m\u00e9todo para la s\u00edntesis de biarilos a trav\u00e9s de reacciones radic\u00e1licas intramoleculares empleando para ello ttmss y aibn empleando como material de partida sulfonamidas diferentemente sustituidas. Los biarilos fueron obtenidos por ipso-sustituci\u00f3n y extrusi\u00f3n del aceptor radicalario so2. como extensi\u00f3n de este trabajo se ha extendido la metodolog\u00eda a la arilaci\u00f3n intramolecular de aminopiridinas por ipso-sustituci\u00f3n de carbamatos. finalmente, el m\u00e9todo se ha ampliado, para dar lugar a la obtenci\u00f3n de aminopiridinas fusionadas, por reacci\u00f3n de adici\u00f3n radic\u00e1lica intramolecular de un radical heteroar\u00edlico a un doble o triple enlace.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>N-aminidas de piridinio en reacciones radicalarias<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 N-aminidas de piridinio en reacciones radicalarias <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Aranzazu Sanchez Mu\u00f1oz <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Alcal\u00e1<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 06\/07\/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>builla G\u00f3mez \u00e1lvarez<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Juan  jos\u00e9 Vaquero l\u00f3pez <\/li>\n<li>benito Alcaide ala\u00f1on (vocal)<\/li>\n<li>v\u00edctor Mart\u00edn Garc\u00eda (vocal)<\/li>\n<li>esther Dominguez perez (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Aranzazu Sanchez Mu\u00f1oz En el curso de nuestros estudios en la reactividad de las n-heteroarilaminidas de pirdinio [&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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