{"id":46920,"date":"2020-01-26T01:40:38","date_gmt":"2020-01-26T01:40:38","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/derivados-del-1-azabutadieno-en-la-sintesis-de-sistemas-heterociclicos-reacciones-electrociclicas-y-de-condensacion\/"},"modified":"2020-01-26T01:40:38","modified_gmt":"2020-01-26T01:40:38","slug":"derivados-del-1-azabutadieno-en-la-sintesis-de-sistemas-heterociclicos-reacciones-electrociclicas-y-de-condensacion","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/quimica\/derivados-del-1-azabutadieno-en-la-sintesis-de-sistemas-heterociclicos-reacciones-electrociclicas-y-de-condensacion\/","title":{"rendered":"Derivados del 1-azabutadieno en la sintesis de sistemas heterociclicos. reacciones electrociclicas y de condensacion."},"content":{"rendered":"<h2>Tesis doctoral de <strong>  Rubio Royo Jos\u00e9 Victor <\/strong><\/h2>\n<p>Las diiminas 1 3  obtenidas por reaccion de bases de schiff con nitrilos saturados y tricloruro de aluminio reaccionan con tetraciano-etileno. Los productos obtenidos no son en ningun caso consistentes con los resultantes de un proceso de diels-alder. La reaccion de estos compuestos diiminicos con heterocumulenos ha servido para dilucidar los dos tipos de mecanismos a traves de los cuales reaccionan estos sistemas derivados del azabutadieno  resultando ademas un nuevo metodo de sintesis de pirimidonas y tiopirimidonas. Por otra parte la reaccion de diiminas 1 3 con sulfuro de carbono conduce a una facil sintesis regioselectiva de tiopirimidonas. Asimismo  la reaccion de los sistemas diiminicos con clururos de acido ha abierto la posibilidad de sintetizar 6h 1 3-oxazinas  compuestos que son practicamente desconocidos en la bibliografia. De los resultados expuestos en este trabajo  se puede sacar la conclusion que  las diiminas 1 3 reaccionan segun procesos electrociclicos o de condensacion.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Derivados del 1-azabutadieno en la sintesis de sistemas heterociclicos. reacciones electrociclicas y de condensacion.<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Derivados del 1-azabutadieno en la sintesis de sistemas heterociclicos. reacciones electrociclicas y de condensacion. <\/li>\n<li><strong>Autor:<\/strong>\u00a0  Rubio Royo Jos\u00e9 Victor <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Oviedo<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 01\/01\/1980<\/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: Jos\u00e9 Joaquin Barluenga Mur <\/li>\n<li>Heinz Hoberg (vocal)<\/li>\n<li>Joaquin Pascual Teresa (vocal)<\/li>\n<li>Angel Alberola Figuerola (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Rubio Royo Jos\u00e9 Victor Las diiminas 1 3 obtenidas por reaccion de bases de schiff con nitrilos [&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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