{"id":8437,"date":"1995-01-01T00:00:00","date_gmt":"1995-01-01T00:00:00","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/1995\/01\/01\/estereoselectividad-de-las-reacciones-de-reduccion-y-adicion-de-organometalicos-a-2-p-tolilsulfinilcicloalcanonas-enantiomericamente-puras\/"},"modified":"1995-01-01T00:00:00","modified_gmt":"1995-01-01T00:00:00","slug":"estereoselectividad-de-las-reacciones-de-reduccion-y-adicion-de-organometalicos-a-2-p-tolilsulfinilcicloalcanonas-enantiomericamente-puras","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/quimica\/estereoselectividad-de-las-reacciones-de-reduccion-y-adicion-de-organometalicos-a-2-p-tolilsulfinilcicloalcanonas-enantiomericamente-puras\/","title":{"rendered":"Estereoselectividad de las reacciones de reduccion y adicion de organometalicos a 2-p-tolilsulfinilcicloalcanonas enantiomericamente puras."},"content":{"rendered":"<h2>Tesis doctoral de <strong> Ana Belen Bueno Melendo <\/strong><\/h2>\n<p>El grupo p-tolueno sulfinilo ha sido utilizado para la induccion de quiralidad en reacciones de reduccion y adicion nucleofila a carbonilo. Las reacciones de formacion de cicloalcanoles tanto secundarios como terciarios ha transcurrido con excelente estereoselectividad. Los hidroxisulfoxidos obtenidos han sido convertidos, por transformaciones sencillas del grupo sulfinilo en intermedios sinteticos de interes como cicloalquenoles y cicloalcanoles 3-sustituidos, estos ultimos obtenidos con elevadas estereoselectividades y buenos rendimientos.  por ultimo, la puesta a punto de esta metodolog\u00eda ha permitido la sintesis de dos productos naturales: en primer lugar se ha obtenido en dos etapas la 4-metil-4-hidroxiciclohex-2-en-1-ona, componente volatil de plantas utilizado como aditivo de perfumes y jabones; en segundo lugar, se ha llevado a cabo una sintesis formal de la manostatina a, inhibidor de glicosidasa, y con posible actividad antiviral.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Estereoselectividad de las reacciones de reduccion y adicion de organometalicos a 2-p-tolilsulfinilcicloalcanonas enantiomericamente puras.<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Estereoselectividad de las reacciones de reduccion y adicion de organometalicos a 2-p-tolilsulfinilcicloalcanonas enantiomericamente puras. <\/li>\n<li><strong>Autor:<\/strong>\u00a0 Ana Belen Bueno Melendo <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 Aut\u00f3noma de Madrid<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 01\/01\/1995<\/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 Luis Garc\u00eda Ruano<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Juan Galvis <\/li>\n<li>Eusebio Juaristi (vocal)<\/li>\n<li>Jes\u00fas Rodriguez (vocal)<\/li>\n<li>Joaquin Plumet (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Ana Belen Bueno Melendo El grupo p-tolueno sulfinilo ha sido utilizado para la induccion de quiralidad en [&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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