{"id":109725,"date":"2011-01-07T00:00:00","date_gmt":"2011-01-07T00:00:00","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/sa%c2%adntesis-de-p-peroxiquinoles-y-p-quinoles-empleando-oxono-como-fuente-de-oxa%c2%adgeno-singlete-estudio-metodologico-y-aplicaciones-sinteticas\/"},"modified":"2011-01-07T00:00:00","modified_gmt":"2011-01-07T00:00:00","slug":"sa%c2%adntesis-de-p-peroxiquinoles-y-p-quinoles-empleando-oxono-como-fuente-de-oxa%c2%adgeno-singlete-estudio-metodologico-y-aplicaciones-sinteticas","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/quimica-organica\/sa%c2%adntesis-de-p-peroxiquinoles-y-p-quinoles-empleando-oxono-como-fuente-de-oxa%c2%adgeno-singlete-estudio-metodologico-y-aplicaciones-sinteticas\/","title":{"rendered":"S\u00edntesis de p-peroxiquinoles y p-quinoles empleando oxono como fuente de ox\u00edgeno singlete. estudio metodol\u00f3gico y aplicaciones sint\u00e9ticas."},"content":{"rendered":"<h2>Tesis doctoral de <strong> Silvia Barradas Mora <\/strong><\/h2>\n<p>La reacci\u00f3n de desaromatizaci\u00f3n oxidante de fenoles para alquil sustituido es un arma poderiosa para acceder de forma sencilla a para quinoles comoel producto natural cochinchinenona. Adem\u00e1s, el tratamiento secuencial de los para-peroxiquinoles y para-quinoles asi sintetizados con \u00e1cido y base permite acceder de froma r\u00e1pida y eficiente a estrocturas de hidrobenzofurano e hibrbenzofuranos polixigenados. Adicionalmente, la rustura oxidativa de los biciclo citados  permite acceder a macrocetolactonas como el cefalospor\u00f3lido c y su ep\u00edmero.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>S\u00edntesis de p-peroxiquinoles y p-quinoles empleando oxono como fuente de ox\u00edgeno singlete. estudio metodol\u00f3gico y aplicaciones sint\u00e9ticas.<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 S\u00edntesis de p-peroxiquinoles y p-quinoles empleando oxono como fuente de ox\u00edgeno singlete. estudio metodol\u00f3gico y aplicaciones sint\u00e9ticas. <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Silvia Barradas Mora <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Aut\u00f3noma de Madrid<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 01\/07\/2011<\/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>Antonio Urbano Pujol<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: benito Alcaide ala\u00f1on <\/li>\n<li>alfonso Fern\u00e1ndez-mayoralas \u00e1lvarez (vocal)<\/li>\n<li>anna Barattucci (vocal)<\/li>\n<li>Mar\u00eda  dolores Badia urrestarazu (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Silvia Barradas Mora La reacci\u00f3n de desaromatizaci\u00f3n oxidante de fenoles para alquil sustituido es un arma poderiosa [&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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