{"id":93941,"date":"2009-12-06T00:00:00","date_gmt":"2009-12-06T00:00:00","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/sa%c2%adntesis-de-compuestos-heteroca%c2%adclicos-a-traves-de-reacciones-en-cascada-catalizadas-por-complejos-de-paladio\/"},"modified":"2009-12-06T00:00:00","modified_gmt":"2009-12-06T00:00:00","slug":"sa%c2%adntesis-de-compuestos-heteroca%c2%adclicos-a-traves-de-reacciones-en-cascada-catalizadas-por-complejos-de-paladio","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/compuestos-organometalicos\/sa%c2%adntesis-de-compuestos-heteroca%c2%adclicos-a-traves-de-reacciones-en-cascada-catalizadas-por-complejos-de-paladio\/","title":{"rendered":"S\u00edntesis de compuestos heteroc\u00edclicos a trav\u00e9s de reacciones en cascada catalizadas por complejos de paladio"},"content":{"rendered":"<h2>Tesis doctoral de <strong> Agust\u00edn Jim\u00e9nez Aquino <\/strong><\/h2>\n<p>En esta memoria se aborda el estudio de nuevas aplicaciones sint\u00e9ticas de las reacciones de acoplamiento cruzado catalizadas por paladio a la s\u00edntesis de compuestos heteroc\u00edclicos. la memoria se encuentra dividida en tres cap\u00edtulos: s\u00edntesis multicomponente de piridinas 2,3,5-trisustituidas, s\u00edntesis modular de indoles a partir de iminas y nuevas reacciones de carbometalaci\u00f3n con iminas.  en el primer cap\u00edtulo se muestra la s\u00edntesis de piridinas trisustituidas a trav\u00e9s de un proceso multicomponente. La formaci\u00f3n de los productos supone dos reacciones de acoplamiento cruzado independientes promovidas por la misma especie catal\u00edtica de paladio seguida de una reacci\u00f3n de cicloadici\u00f3n [4+2]. en el segundo cap\u00edtulo se describe una nueva metodolog\u00eda general para la s\u00edntesis de indoles a trav\u00e9s de un proceso en cascada catalizado por paladio. El cap\u00edtulo se encuentra dividido en tres partes: parte a: aborda la s\u00edntesis de indoles a partir de iminas y o-dihaloarenos; parte b: se extiende al empleo de sulfonatos de o-clorobenceno como electr\u00f3filos y representa una s\u00edntesis indirecta de indoles a partir de fenoles; parte c: recoge los resultados obtenidos cuando se lleva a cabo la reacci\u00f3n en suspensi\u00f3n acuosa y bajo radiaci\u00f3n microondas. finalmente, en el tercer cap\u00edtulo se muestran los primeros ejemplos en los que una imina participa como componente nucle\u00f3filo en una reacci\u00f3n de carbopaladaci\u00f3n catal\u00edtica que conduce a la obtenci\u00f3n de dihidropirroles.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>S\u00edntesis de compuestos heteroc\u00edclicos a trav\u00e9s de reacciones en cascada catalizadas por complejos de paladio<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 S\u00edntesis de compuestos heteroc\u00edclicos a trav\u00e9s de reacciones en cascada catalizadas por complejos de paladio <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Agust\u00edn Jim\u00e9nez Aquino <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Oviedo<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 12\/06\/2009<\/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>Jos\u00e9 Joaquin Barluenga Mur<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: rafael Suau suarez <\/li>\n<li>alfredo Mart\u00edn fuentes (vocal)<\/li>\n<li>Jos\u00e9 Luis Mascare\u00f1as cid (vocal)<\/li>\n<li>Ana S\u00e1nchez-migall\u00f3n bermejo (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Agust\u00edn Jim\u00e9nez Aquino En esta memoria se aborda el estudio de nuevas aplicaciones sint\u00e9ticas de las reacciones [&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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