{"id":49733,"date":"2021-05-06T13:58:28","date_gmt":"2021-05-06T13:58:28","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/polianiones-organoalcalinos-betafuncionalizados-nuevos-reactivos-en-sintesis-organica\/"},"modified":"2021-05-06T13:58:28","modified_gmt":"2021-05-06T13:58:28","slug":"polianiones-organoalcalinos-betafuncionalizados-nuevos-reactivos-en-sintesis-organica","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/quimica\/polianiones-organoalcalinos-betafuncionalizados-nuevos-reactivos-en-sintesis-organica\/","title":{"rendered":"Polianiones organoalcalinos betafuncionalizados. nuevos reactivos en sintesis organica."},"content":{"rendered":"<h2>Tesis doctoral de <strong> Jorge Villama\u00f1a Garcia <\/strong><\/h2>\n<p>Se ha estudiado la reactividad de dianiones organoalcalinos del tipo c-(y-) frente a bromuros de alanilo  disulfuro de dimetico e iminas. Se han preparado trianiones del tipo c-c(y-)c- organoalcalinos  se ha estudiado su estabilidad y reaccion simultanea o sucesiva con electrofilos (agua  oxido de deuterio  bromuro de etilo  disulfuro de dimetilo  trimetilclorosilano). Se han obtenido trianiones del tipo c(x-)c-c(y-) y c(x-)c(y-)c- organualcalinos  se ha estudiado su estabilidad termica e inicialmente su comportamiento frente a electrofilos. Se ha preparado un tetraanion del tipo c-c(y-)c(y-)c- derivado de litio  etudiado su estabilidad termica y de forma inicial su reactividad frente a electrofilos. El metodogeneral de obtencion de estas polianiones es una reaccion de transmetalacion mercurio-metal alcalino a partir de ciompuestos organomercurios funcionalizados.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Polianiones organoalcalinos betafuncionalizados. nuevos reactivos en sintesis organica.<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Polianiones organoalcalinos betafuncionalizados. nuevos reactivos en sintesis organica. <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Jorge Villama\u00f1a Garcia <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Oviedo<\/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>Jos\u00e9 Joaquin Barluenga Mur<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Fermin Gomez Beltran <\/li>\n<li>Jos\u00e9 Joaquin Barluenga Mur (vocal)<\/li>\n<li>\u00e1ngel Alberola Figueroa (vocal)<\/li>\n<li>Vicente Gotor Santamar\u00eda (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Jorge Villama\u00f1a Garcia Se ha estudiado la reactividad de dianiones organoalcalinos del tipo c-(y-) frente a bromuros [&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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