{"id":104952,"date":"2018-03-11T10:28:18","date_gmt":"2018-03-11T10:28:18","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/hidroxiamidas-vs-aminoalcoholes-como-ligandos-quirales-para-la-adicionenantioselectiva-de-reactivos-organozincicos-a-aldehidos\/"},"modified":"2018-03-11T10:28:18","modified_gmt":"2018-03-11T10:28:18","slug":"hidroxiamidas-vs-aminoalcoholes-como-ligandos-quirales-para-la-adicionenantioselectiva-de-reactivos-organozincicos-a-aldehidos","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/quimica\/hidroxiamidas-vs-aminoalcoholes-como-ligandos-quirales-para-la-adicionenantioselectiva-de-reactivos-organozincicos-a-aldehidos\/","title":{"rendered":"Hidroxiamidas vs aminoalcoholes como ligandos quirales para la adici\u00f3nenantioselectiva de reactivos organozincicos a aldehidos."},"content":{"rendered":"<h2>Tesis doctoral de <strong> Tom\u00e1s De Las Casas Engel <\/strong><\/h2>\n<p>La tesis versa sobre el desarrollo de hidroxiamidas quirales, concretamente 10-amino-10-oxoisoborneoles, como ligandos de f\u00e1cil acceso sint\u00e9tico para la adici\u00f3n enantioselectiva de reactivos organoz\u00edncicos a aldeh\u00eddos. En este sentido, se describe un  estudio de los factores estructurales clave que rigen la actividad catal\u00edtica en este tipo de ligandos, que se realiza en comparaci\u00f3n con los de los correspondientes amino alcoholes (10-aminoisoborneoles). Los resultados alcanzados suponen un avance  en el conocimiento del origen de la actividad catal\u00edtica en ambos tipos de ligandos (hidroxiamidas vs. Amino alcoholes) y permiten establecer las bases para el dise\u00f1o optimizado de nuevas hidroxiamidas.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Hidroxiamidas vs aminoalcoholes como ligandos quirales para la adici\u00f3nenantioselectiva de reactivos organozincicos a aldehidos.<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Hidroxiamidas vs aminoalcoholes como ligandos quirales para la adici\u00f3nenantioselectiva de reactivos organozincicos a aldehidos. <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Tom\u00e1s De Las Casas Engel <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Complutense de Madrid<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 18\/11\/2010<\/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>Beatriz Lora Maroto<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: joaquin Plumet ortega <\/li>\n<li>Miguel \u00e1ngel Yus astiz (vocal)<\/li>\n<li>gonzalo Blay llinares (vocal)<\/li>\n<li>rosario Fernandez fernandez (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Tom\u00e1s De Las Casas Engel La tesis versa sobre el desarrollo de hidroxiamidas quirales, concretamente 10-amino-10-oxoisoborneoles, como [&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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