{"id":8452,"date":"1995-01-01T00:00:00","date_gmt":"1995-01-01T00:00:00","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/1995\/01\/01\/sintesis-de-47-diamino-29dimetil-1112-dihidro-5h-5611-a-triazanaftaceno-y-sus-derivados-reconocimiento-de-carboxilatos-y-autoasociacion\/"},"modified":"1995-01-01T00:00:00","modified_gmt":"1995-01-01T00:00:00","slug":"sintesis-de-47-diamino-29dimetil-1112-dihidro-5h-5611-a-triazanaftaceno-y-sus-derivados-reconocimiento-de-carboxilatos-y-autoasociacion","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/quimica\/sintesis-de-47-diamino-29dimetil-1112-dihidro-5h-5611-a-triazanaftaceno-y-sus-derivados-reconocimiento-de-carboxilatos-y-autoasociacion\/","title":{"rendered":"Sintesis de 4,7-diamino-2,9dimetil-11,12-dihidro-(5h) -5,6,11-a-triazanaftaceno y sus derivados: reconocimiento de carboxilatos y autoasociacion."},"content":{"rendered":"<h2>Tesis doctoral de <strong>  Chicharro Santamaria Jos\u00e9 Luis <\/strong><\/h2>\n<p>Como se ha demostrado previamente las guanidinas biciclicas forman excelentes receptores para la complejacion de oxoaniones. En esta memoria se ha sintetizado una unidad de guanidina biciclica aromatica con grupos aminos en los que se han introducido restos de d- y l-aminoacidos para dar lugar a receptores de aminoacidos n-protegidos. Realizandose estudios de complejacion enantioselectiva y selectivas con este tipo de sustratos. Tambien se ha preparado un receptor de peptidos, formado por una unidad de diaminodibenzoguanidina con un espaciador (diacido) y una unidad peptidica de tetraisoleucina amino libre. Por ultimo se ha llevado a cabo la aproximacion a la sintesis de un catenando, aprovechando la caracteristica observada a lo largo de la realizacion de dicha memoria del grupo guanidina en generar dimeros en forma de u.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Sintesis de 4,7-diamino-2,9dimetil-11,12-dihidro-(5h) -5,6,11-a-triazanaftaceno y sus derivados: reconocimiento de carboxilatos y autoasociacion.<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Sintesis de 4,7-diamino-2,9dimetil-11,12-dihidro-(5h) -5,6,11-a-triazanaftaceno y sus derivados: reconocimiento de carboxilatos y autoasociacion. <\/li>\n<li><strong>Autor:<\/strong>\u00a0  Chicharro Santamaria Jos\u00e9 Luis <\/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\/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> Mendoza Sans Francisco Javier<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Ernest Giralt Lledo <\/li>\n<li>Pedro Molina Buend\u00eda (vocal)<\/li>\n<li>Miguel \u00e1ngel Yus Astiz (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 Chicharro Santamaria Jos\u00e9 Luis Como se ha demostrado previamente las guanidinas biciclicas forman excelentes receptores para la [&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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