{"id":41679,"date":"1999-01-01T00:00:00","date_gmt":"1999-01-01T00:00:00","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/sintesis-de-sr-p-tolilsulfinilmetilquinoles-estudio-de-sus-reacciones-de-diels-alder-y-de-adicion-de-compuestos-organoaluminicos\/"},"modified":"1999-01-01T00:00:00","modified_gmt":"1999-01-01T00:00:00","slug":"sintesis-de-sr-p-tolilsulfinilmetilquinoles-estudio-de-sus-reacciones-de-diels-alder-y-de-adicion-de-compuestos-organoaluminicos","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/quimica\/sintesis-de-sr-p-tolilsulfinilmetilquinoles-estudio-de-sus-reacciones-de-diels-alder-y-de-adicion-de-compuestos-organoaluminicos\/","title":{"rendered":"Sintesis de (s)r-(p-tolilsulfinilmetilquinoles): estudio de sus reacciones de diels-alder y de adicion de compuestos organoaluminicos."},"content":{"rendered":"<h2>Tesis doctoral de <strong> Manuel Perez Gonzalez <\/strong><\/h2>\n<p>El estudio de las reacciones de diels-alder de los p-quinoles con ciclopentadieno y piperileno, ha puesto de manifiesto un comportamiento altamente estereoselectivo de estos filodienos.  la transferencia de grupos alguilo, vinilo o acetil\u00e9nicos a partir de los organoalanos correspondientes se ha revelado totalmente general. La reacci\u00f3n permite generar centros estereog\u00e9nicos con total control de la distereoselectividad.  la \u00faltima parte se ha centrado en la aplicaci\u00f3n de los resultados obtenidos a la s\u00edntesis de productos naturales de inter\u00e9s biol\u00f3gico..<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Sintesis de (s)r-(p-tolilsulfinilmetilquinoles): estudio de sus reacciones de diels-alder y de adicion de compuestos organoaluminicos.<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Sintesis de (s)r-(p-tolilsulfinilmetilquinoles): estudio de sus reacciones de diels-alder y de adicion de compuestos organoaluminicos. <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Manuel Perez Gonzalez <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Aut\u00f3noma de Madrid<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 01\/01\/1999<\/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>Mar\u00eda  Del Carmen Carre\u00f1o Garcia<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Jos\u00e9 Luis Garc\u00eda ruano <\/li>\n<li>rosa Calramunt vallespi (vocal)<\/li>\n<li>Miguel \u00e1ngel Yus astiz (vocal)<\/li>\n<li>benito Alcaide ala\u00f1on (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Manuel Perez Gonzalez El estudio de las reacciones de diels-alder de los p-quinoles con ciclopentadieno y piperileno, [&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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