{"id":50128,"date":"2021-06-06T20:45:03","date_gmt":"2021-06-06T20:45:03","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/comportamiento-de-las-aziridinas-frente-a-compuestos-organoaluminicos\/"},"modified":"2021-06-06T20:45:03","modified_gmt":"2021-06-06T20:45:03","slug":"comportamiento-de-las-aziridinas-frente-a-compuestos-organoaluminicos","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/quimica\/comportamiento-de-las-aziridinas-frente-a-compuestos-organoaluminicos\/","title":{"rendered":"Comportamiento de las aziridinas frente a compuestos organoaluminicos"},"content":{"rendered":"<h2>Tesis doctoral de <strong> Antonio P\u00e9rez Serrano <\/strong><\/h2>\n<p>Por reaccion de 2 2-difenil-3-metilaziridina 2-etil-2-fenil-3-metilaziridina 2-fenil-2-isopropil-3-metilaziridina cis-2-fenil-3-metilaziridina  2-etil-2-fenil-aziridina frente a tricloruro de aluminio  trietilaluminio triisobutilaluminio  cloruro de dietilaluminio  dicloruro de etilaluminio  cloruro de diisobutilaluminio  y dicloruro de isobutilaluminio en distintos disolventes se obtienen aldehidos  cetonas  aminas y alfa-hidroxiaminas provenientes  en general  de reacciones de apertura del anillo aziridinico con transposicion de los sustituyentes de este. La reactividad observada depende de la acidez de lewis relativa de los organoaluminicos empleados para cada aziridina. Asimismo la reactividad comparada con la de epoxidos en este tipo de reacciones es menor.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Comportamiento de las aziridinas frente a compuestos organoaluminicos<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Comportamiento de las aziridinas frente a compuestos organoaluminicos <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Antonio P\u00e9rez Serrano <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Valladolid<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 01\/01\/1982<\/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>\u00e1ngel Alberola Figueroa<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: \u00e1ngel Alberola Figueroa <\/li>\n<li>Victor Riera Gonz\u00e1lez (vocal)<\/li>\n<li>Jos\u00e9 Joaquin Barluenga Mur (vocal)<\/li>\n<li>Eladio Montoya Melgar (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Antonio P\u00e9rez Serrano Por reaccion de 2 2-difenil-3-metilaziridina 2-etil-2-fenil-3-metilaziridina 2-fenil-2-isopropil-3-metilaziridina cis-2-fenil-3-metilaziridina 2-etil-2-fenil-aziridina frente a tricloruro de aluminio [&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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