{"id":6960,"date":"1995-01-01T00:00:00","date_gmt":"1995-01-01T00:00:00","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/1995\/01\/01\/2-amino-13-butadienos-reactividad-frente-a-carbenos-estabilizados-por-metales-del-grupo-6\/"},"modified":"1995-01-01T00:00:00","modified_gmt":"1995-01-01T00:00:00","slug":"2-amino-13-butadienos-reactividad-frente-a-carbenos-estabilizados-por-metales-del-grupo-6","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/quimica\/2-amino-13-butadienos-reactividad-frente-a-carbenos-estabilizados-por-metales-del-grupo-6\/","title":{"rendered":"2-amino-1,3-butadienos: reactividad frente a carbenos estabilizados por metales del grupo 6"},"content":{"rendered":"<h2>Tesis doctoral de <strong>  Martin Fuentes Jos\u00e9 Alfredo <\/strong><\/h2>\n<p>La memoria esta dedicada al estudio de la reactividad de los 2-aminodienos frente a los complejos carbeno de metales del grupo 6. En el primer capitulo se estudia la reactividad frente a los complejos aril oxicarbeno. Se pone a punto un nuevo metodo de preparacion de amino vinilcarbenos y se estudia el comportamiento de estos en los procesos de ciclopropanacion de olefinas con sustituyentes electron-atractores y de anulacion con acetilenos.  el segundo capitulo recoge la reaccion de cicloadicion (4+2) de los 2- aminodienos y los oxi vinilcarbenos de wolframio para dar lugar a derivados de la ciclohexanona que aun contienen la funcionalidad carbeno.  el capitulo 3 versa sobre la reaccion entre los 2-aminodienos y los oxi vinilcarbenos de cromo, que da lugar a nuevos carbociclos de siete eslabones.  por ultimo, en el cuarto capitulo se presentan algunas de las reacciones indicadas en los capitulos 2 y 3 pero empleando 2-aminodienos quirales.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>2-amino-1,3-butadienos: reactividad frente a carbenos estabilizados por metales del grupo 6<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 2-amino-1,3-butadienos: reactividad frente a carbenos estabilizados por metales del grupo 6 <\/li>\n<li><strong>Autor:<\/strong>\u00a0  Martin Fuentes Jos\u00e9 Alfredo <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Oviedo<\/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>Jos\u00e9 Joaquin Barluenga Mur<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Julio Delgado Mart\u00edn <\/li>\n<li>Josep Mar\u00eda Moret\u00f3 Canela (vocal)<\/li>\n<li>Miguel \u00e1ngel Peric\u00ed\u00a0s Brondo (vocal)<\/li>\n<li> Sierra Rodriguez Miguel Angel (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Martin Fuentes Jos\u00e9 Alfredo La memoria esta dedicada al estudio de la reactividad de los 2-aminodienos frente [&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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