{"id":10585,"date":"1996-01-01T00:00:00","date_gmt":"1996-01-01T00:00:00","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/1996\/01\/01\/nucleosidos-carbociclicos-12-disustituidos\/"},"modified":"1996-01-01T00:00:00","modified_gmt":"1996-01-01T00:00:00","slug":"nucleosidos-carbociclicos-12-disustituidos","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/ciencias-medicas\/nucleosidos-carbociclicos-12-disustituidos\/","title":{"rendered":"Nucleosidos carbociclicos 1,2-disustituidos."},"content":{"rendered":"<h2>Tesis doctoral de <strong> Marta Teijeira Bautista <\/strong><\/h2>\n<p>En esta memoria se presenta un gran numero de nuevos compuestos bien elegidos y bien caracterizados, y sintetizados mediante rutas sinteticas muy directas y versatiles. Estos analogos carbociclicos de nucleosidos, son productos de un gran interes como quimioterapicos, parcialmente demostrado ya como antivirales, pero tambien como anticancer.  se trata de una serie en la que se estudia fundamentalmente una modificacion estructural original dentro de su campo. La serie es muy amplia y explora diferencias estereoquimicas en el carbociclo, en la union entre el carbociclo y la base heterociclica y tambien modificaciones de la base.  se destaca tambien el estudio estructural realizado, que si bien es inicial en la tesis, ofrece resultados significativos y muy interesantes.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Nucleosidos carbociclicos 1,2-disustituidos.<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Nucleosidos carbociclicos 1,2-disustituidos. <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Marta Teijeira Bautista <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Santiago de compostela<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 01\/01\/1996<\/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>Lourdes Santana Pen\u00edn<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Julio \u00e1lvarez-builla G\u00f3mez <\/li>\n<li>Antonio Torres (vocal)<\/li>\n<li>Manlio Palumbo (vocal)<\/li>\n<li>Sergio Castillon (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Marta Teijeira Bautista En esta memoria se presenta un gran numero de nuevos compuestos bien elegidos y [&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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