{"id":5484,"date":"1995-01-01T00:00:00","date_gmt":"1995-01-01T00:00:00","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/1995\/01\/01\/estudio-de-las-reacciones-de-cicloadicion-de-compuestos-estirenicos-y-analogos-heterociclicos-con-bencino\/"},"modified":"1995-01-01T00:00:00","modified_gmt":"1995-01-01T00:00:00","slug":"estudio-de-las-reacciones-de-cicloadicion-de-compuestos-estirenicos-y-analogos-heterociclicos-con-bencino","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/quimica\/estudio-de-las-reacciones-de-cicloadicion-de-compuestos-estirenicos-y-analogos-heterociclicos-con-bencino\/","title":{"rendered":"Estudio de las reacciones de cicloadicion de compuestos estirenicos y analogos heterociclicos con bencino."},"content":{"rendered":"<h2>Tesis doctoral de <strong> Sonsoles Perez Santamaria <\/strong><\/h2>\n<p>La memoria muestra la reactividad de diferentes derivados del estireno en la reaccion de cicloadicion (4+2) frente al bencino, y evalua la posible utilidad sintetica del procedimiento. A continuacion trata el estudio de la reactividad de analogos heterociclicos del estireno. Como sustratos dienicos se prepararon 2-vinil y 3-vinil derivados de los anillos de furano, pirrol y tiofeno, respectivamente, lo cual permite comparar el distinto comportamiento de estos tres ciclos en funcion de la naturaleza del heteroatomo. En ultimo lugar se ensaya la cicloadicion intramolecular con bencino de oxazoles.  en resumen, se ha estudiado la reactividad de diferentes derivados estirenicos y analogos heterociclicos frente al bencino, obteniendose compuestos con esqueletos fenantrenico, naftoheterociclico, norbornanico y naftalenicos. Este procedimiento sintetico puede ser aplicado a la preparacion de aporfinoides, asi como a la preparacion de derivados con estructuras de interes farmacologico.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Estudio de las reacciones de cicloadicion de compuestos estirenicos y analogos heterociclicos con bencino.<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Estudio de las reacciones de cicloadicion de compuestos estirenicos y analogos heterociclicos con bencino. <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Sonsoles Perez Santamaria <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Santiago de compostela<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 01\/01\/1995<\/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>Enrique Guitian Rivera<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Josep Font Cierco <\/li>\n<li>Jos\u00e9 Luis Garc\u00eda Ruano (vocal)<\/li>\n<li>Guillermo Mart\u00ednez Massanet (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 Sonsoles Perez Santamaria La memoria muestra la reactividad de diferentes derivados del estireno en la reaccion 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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