{"id":74080,"date":"2018-03-09T23:19:02","date_gmt":"2018-03-09T23:19:02","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/adicion-de-reactivos-organometalicos-y-reacciones-13-dipolares-con-nitronas-quirales-derivadas-de-eritrulosa\/"},"modified":"2018-03-09T23:19:02","modified_gmt":"2018-03-09T23:19:02","slug":"adicion-de-reactivos-organometalicos-y-reacciones-13-dipolares-con-nitronas-quirales-derivadas-de-eritrulosa","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/quimica\/adicion-de-reactivos-organometalicos-y-reacciones-13-dipolares-con-nitronas-quirales-derivadas-de-eritrulosa\/","title":{"rendered":"Adicion de reactivos organometalicos y reacciones 1,3 dipolares con nitronas quirales derivadas de eritrulosa"},"content":{"rendered":"<h2>Tesis doctoral de <strong> Raul Portoles Garcia <\/strong><\/h2>\n<p>En la presente tesis se han preparado nitronas derivadas de 3,4-o-isopropiliden-l-eritrulosa. se ha estudiado la reactividad de las mismas frente a la reacci\u00f3n de adici\u00f3n de compuestos organomet\u00e1licos. Se han obtenido en determinadas condiciones elevadas diastereoselectividades para la adici\u00f3n de especies nucleof\u00edlicas. la configuraci\u00f3n absoluta de los diastereois\u00f3meros obtenidos se ha realizado mediante t\u00e9cnicas de difracci\u00f3n de rayos-x de monocristal, mediante correlaci\u00f3n qu\u00edmica con compuestos de estructuras conocidas y mediante estudios espectrosc\u00f3picos de derivados r\u00edgidos. Los productos de adici\u00f3n se han transformado en a-alquil-n-acetoxi-a-aminoesteres y (r)-a-metilserina. Asimismo se han estudiado reacciones de cicloadici\u00f3n 1,3-dipolares entre las nitronas (dipolos) y dipolar\u00f3filos de diferente naturaleza electr\u00f3nica.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Adicion de reactivos organometalicos y reacciones 1,3 dipolares con nitronas quirales derivadas de eritrulosa<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Adicion de reactivos organometalicos y reacciones 1,3 dipolares con nitronas quirales derivadas de eritrulosa <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Raul Portoles Garcia <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Jaume i de castell\u00f3n<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 20\/05\/2005<\/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>Juan Murga Clausell<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Jaime Primo millo <\/li>\n<li>Jos\u00e9 ram\u00f3n Pedro llinares (vocal)<\/li>\n<li>mercedes Amat tus\u00f3n (vocal)<\/li>\n<li>Juan  Francisco Sanz cervera (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Raul Portoles Garcia En la presente tesis se han preparado nitronas derivadas de 3,4-o-isopropiliden-l-eritrulosa. se ha estudiado [&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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