{"id":129757,"date":"1996-01-01T00:00:00","date_gmt":"1996-01-01T00:00:00","guid":{"rendered":"https:\/\/www.deberes.net\/tesis\/sin-categoria\/sintesis-de-di-y-tri-oxaespiroacetales-quirales-reagrupamiento-de-dioxaespiroacetales-a-sistemas-cis-y-trans-16-dioxadecalinicos\/"},"modified":"1996-01-01T00:00:00","modified_gmt":"1996-01-01T00:00:00","slug":"sintesis-de-di-y-tri-oxaespiroacetales-quirales-reagrupamiento-de-dioxaespiroacetales-a-sistemas-cis-y-trans-16-dioxadecalinicos","status":"publish","type":"post","link":"https:\/\/www.deberes.net\/tesis\/quimica\/sintesis-de-di-y-tri-oxaespiroacetales-quirales-reagrupamiento-de-dioxaespiroacetales-a-sistemas-cis-y-trans-16-dioxadecalinicos\/","title":{"rendered":"Sintesis de di- y tri-oxaespiroacetales quirales. reagrupamiento de dioxaespiroacetales a sistemas cis- y trans-1,6-dioxadecalinicos."},"content":{"rendered":"<h2>Tesis doctoral de <strong>  Martin Hernandez M. Angeles <\/strong><\/h2>\n<p>Se ha desarrollado una nueva metodolog\u00eda para la sintesis de espiroacetales quirales a partir de carbohidratos, via una abstraccion intramolecular de hidrogeno promovida por radicales alcoxidos generados a partir de alcoholes por fotolisis en presencia de (diacetoxiyodo) benceno y yodo.Se han obtenido derivados quirales de los sistemas 1,6-dioxaespiro (4.4) nonano, 1,6-dioxaespiro (4.5) decano y 1,7-dioxaespiro (5.5) undecano.Esta metodolog\u00eda se ha extendido a la preparacion del sistema 1,6,8- trioxadiespiro (4.1.5.3) pentadecano.Tambien se ha desarrollado un nuevo metodo para la sintesis de 1,6-dioxadecalinas cis- y trans-fusionadas por reagrupamiento de x-hidroxiespiroacetales.<\/p>\n<p>&nbsp;<\/p>\n<h3>Datos acad\u00e9micos de la tesis doctoral \u00ab<strong>Sintesis de di- y tri-oxaespiroacetales quirales. reagrupamiento de dioxaespiroacetales a sistemas cis- y trans-1,6-dioxadecalinicos.<\/strong>\u00ab<\/h3>\n<ul>\n<li><strong>T\u00edtulo de la tesis:<\/strong>\u00a0 Sintesis de di- y tri-oxaespiroacetales quirales. reagrupamiento de dioxaespiroacetales a sistemas cis- y trans-1,6-dioxadecalinicos. <\/li>\n<li><strong>Autor:<\/strong>\u00a0  Martin Hernandez M. Angeles <\/li>\n<li><strong>Universidad:<\/strong>\u00a0 La laguna<\/li>\n<li><strong>Fecha de lectura de la tesis:<\/strong>\u00a0 01\/01\/1996<\/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>Ernesto Suarez L\u00f3pez<\/li>\n<\/ul>\n<\/li>\n<li><strong>Tribunal<\/strong>\n<ul>\n<li>Presidente del tribunal: Manuel Dabrio Ba\u00f1uls <\/li>\n<li>Teodor Parella Coll (vocal)<\/li>\n<li>Jos\u00e9 Adri\u00e1n Gav\u00edn Sazatornil (vocal)<\/li>\n<li>Jos\u00e9 Darias Jerez (vocal)<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>&nbsp;<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Tesis doctoral de Martin Hernandez M. Angeles Se ha desarrollado una nueva metodolog\u00eda para la sintesis de espiroacetales quirales a [&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 center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-gradient":""},"tablet":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-gradient":""},"mobile":{"background-color":"","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-gradient":""}},"ast-content-background-meta":{"desktop":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-gradient":""},"tablet":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-gradient":""},"mobile":{"background-color":"var(--ast-global-color-5)","background-image":"","background-repeat":"repeat","background-position":"center center","background-size":"auto","background-attachment":"scroll","background-type":"","background-media":"","overlay-type":"","overlay-color":"","overlay-gradient":""}},"footnotes":""},"categories":[1648,9915,17,416,415],"tags":[9943,10041,9944,1966,243196,78288],"class_list":["post-129757","post","type-post","status-publish","format-standard","hentry","category-estructura-de-moleculas-organicas","category-la-laguna","category-quimica","category-quimica-organica","category-radicales-libres","tag-ernesto-suarez-lopez","tag-jose-adrian-gavin-sazatornil","tag-jose-darias-jerez","tag-manuel-dabrio-banuls","tag-martin-hernandez-m-angeles","tag-teodor-parella-coll"],"_links":{"self":[{"href":"https:\/\/www.deberes.net\/tesis\/wp-json\/wp\/v2\/posts\/129757","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.deberes.net\/tesis\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.deberes.net\/tesis\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.deberes.net\/tesis\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.deberes.net\/tesis\/wp-json\/wp\/v2\/comments?post=129757"}],"version-history":[{"count":0,"href":"https:\/\/www.deberes.net\/tesis\/wp-json\/wp\/v2\/posts\/129757\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.deberes.net\/tesis\/wp-json\/wp\/v2\/media?parent=129757"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.deberes.net\/tesis\/wp-json\/wp\/v2\/categories?post=129757"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.deberes.net\/tesis\/wp-json\/wp\/v2\/tags?post=129757"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}