{"id":93202,"date":"2009-08-05T00:00:00","date_gmt":"2009-08-05T00:00:00","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/sa%c2%adntesis-enantioselectiva-de-aminoacidos-no-naturales-y-aplicacion-a-la-sa%c2%adntesis-de-peptidos-con-interes-farmacologico\/"},"modified":"2009-08-05T00:00:00","modified_gmt":"2009-08-05T00:00:00","slug":"sa%c2%adntesis-enantioselectiva-de-aminoacidos-no-naturales-y-aplicacion-a-la-sa%c2%adntesis-de-peptidos-con-interes-farmacologico","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/quimica-organica\/sa%c2%adntesis-enantioselectiva-de-aminoacidos-no-naturales-y-aplicacion-a-la-sa%c2%adntesis-de-peptidos-con-interes-farmacologico\/","title":{"rendered":"S\u00edntesis enantioselectiva de amino\u00e1cidos no naturales y aplicaci\u00f3n a la s\u00edntesis de p\u00e9ptidos con inter\u00e9s farmacol\u00f3gico"},"content":{"rendered":"<h2>Tesis doctoral de <strong> Rosario Ram\u00f3n Albalate <\/strong><\/h2>\n<p>La s\u00edntesis de \u00c2\u00bf-amino\u00e1cidos no naturales conformacionalmente restringidos o modificados tienen una importancia creciente, pues a pesar de no ser componentes estructurales de las prote\u00ednas, sus aplicaciones biol\u00f3gicas y terap\u00e9uticas en la s\u00edntesis de f\u00e1rmacos (como parte estructural) y en la s\u00edntesis de p\u00e9ptidos (modificando las propiedades est\u00e9ricas, conformacionales y electr\u00f3nicas) son cada vez m\u00e1s frecuentes. En la presente tesis se plante\u00f3 la s\u00edntesis de diferentes \u00c2\u00bf-amino\u00e1cidos no naturales mediante rutas eficaces que nos permitieran su desarrollo a escala multigramo para su posterior utilizaci\u00f3n en la s\u00edntesis de p\u00e9ptidos con inter\u00e9s farmacol\u00f3gico.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>S\u00edntesis enantioselectiva de amino\u00e1cidos no naturales y aplicaci\u00f3n a la s\u00edntesis de p\u00e9ptidos con inter\u00e9s farmacol\u00f3gico<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 S\u00edntesis enantioselectiva de amino\u00e1cidos no naturales y aplicaci\u00f3n a la s\u00edntesis de p\u00e9ptidos con inter\u00e9s farmacol\u00f3gico <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Rosario Ram\u00f3n Albalate <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Barcelona<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 08\/05\/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>Antoni Riera Escale<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: santos Fustero lardi\u00e9s <\/li>\n<li>david Andreu mart\u00ednez (vocal)<\/li>\n<li>  (vocal)<\/li>\n<li>  (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Rosario Ram\u00f3n Albalate La s\u00edntesis de \u00c2\u00bf-amino\u00e1cidos no naturales conformacionalmente restringidos o modificados tienen una importancia creciente, [&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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