{"id":418,"date":"2016-11-24T19:49:38","date_gmt":"2016-11-24T10:49:38","guid":{"rendered":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/ohmorilab\/?page_id=418"},"modified":"2016-11-28T11:19:32","modified_gmt":"2016-11-28T02:19:32","slug":"total-synthesis-of-natural-product","status":"publish","type":"page","link":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/?page_id=418","title":{"rendered":"Total Synthesis of Natural Product"},"content":{"rendered":"<h3 style=\"text-align: left;\">Out lines for total syntheses<\/h3>\n<ul>\n<li><a href=\"#R000\">mycinamicinIV<\/a><\/li>\n<li><a href=\"#R001\">vineomycinone B2<\/a><\/li>\n<li><a href=\"#R002\">aquayamycin<\/a><\/li>\n<li><a href=\"#R003\">avenaciolide<\/a><\/li>\n<li><a href=\"#R004\">fraquinocins<\/a><\/li>\n<li><a href=\"#R005\">galtamycinone<\/a><\/li>\n<li><a href=\"#R006\">gilvocarcins<\/a><\/li>\n<li><a href=\"#R007\">C104 antibiotic<\/a><\/li>\n<li><a href=\"#R008\">eicosanoid<\/a><\/li>\n<li><a href=\"#R009\">methylerysodienone<\/a><\/li>\n<li><a href=\"#R010\">procyanidins<\/a><\/li>\n<li><a href=\"#R011\">lotthanongine<\/a><\/li>\n<li><a href=\"#R012\">malyngolide<\/a><\/li>\n<li><a href=\"#R013\">seragakinone A<\/a><\/li>\n<li><a href=\"#R014\">BE-43472B<\/a><\/li>\n<li><a href=\"#R015\">saptomycin B<\/a><\/li>\n<li><a href=\"#R016\">cavicularin<\/a><\/li>\n<li><a href=\"#R017\">cinnamtannin B1<\/a><\/li>\n<\/ul>\n<hr \/>\n<h2 id=\"R000\">Total Synthesis of Mycinamicin IV<\/h2>\n<figure class=\"center\"><img decoding=\"async\" src=\"\/ohmorilab\/wp-content\/themes\/org-synth\/image\/total-synth-e\/mycinamicin.png\" alt=\"\" \/><\/figure>\n<h2 id=\"R001\">Total Synthesis of Vineomycinone B2<\/h2>\n<figure class=\"center\"><img decoding=\"async\" src=\"\/ohmorilab\/wp-content\/themes\/org-synth\/image\/total-synth-e\/vineomycinoneB2.png\" alt=\"\" \/><\/figure>\n<h2 id=\"R002\">Total Synthesis of Aquayamycin<\/h2>\n<figure class=\"center\"><img decoding=\"async\" src=\"\/ohmorilab\/wp-content\/themes\/org-synth\/image\/total-synth-e\/aquayamycin.png\" alt=\"\" \/><\/figure>\n<h2 id=\"R003\">Total Synthesis of Avenaciolide<\/h2>\n<figure class=\"center\"><img decoding=\"async\" src=\"\/ohmorilab\/wp-content\/themes\/org-synth\/image\/total-synth-e\/avenaciolide.png\" alt=\"\" \/><\/figure>\n<h2 id=\"R004\">Total Syntheses of Fraquinocins<\/h2>\n<figure class=\"center\"><img decoding=\"async\" src=\"\/ohmorilab\/wp-content\/themes\/org-synth\/image\/total-synth-e\/fraquinocins.png\" alt=\"\" \/><\/figure>\n<h2 id=\"R005\">Total Synthesis of Galtamycinone<\/h2>\n<figure class=\"center\"><img decoding=\"async\" src=\"\/ohmorilab\/wp-content\/themes\/org-synth\/image\/total-synth-e\/galtamycinone.png\" alt=\"\" \/><\/figure>\n<h2 id=\"R006\">Total Syntheses of Gilvocarcins<\/h2>\n<figure class=\"center\"><img decoding=\"async\" src=\"\/ohmorilab\/wp-content\/themes\/org-synth\/image\/total-synth-e\/gilvocarcins.png\" alt=\"\" \/><\/figure>\n<h2 id=\"R007\">Total Synthesis of C104 antibiotic<\/h2>\n<figure class=\"center\"><img decoding=\"async\" src=\"\/ohmorilab\/wp-content\/themes\/org-synth\/image\/total-synth-e\/C104.png\" alt=\"\" \/><\/figure>\n<h2 id=\"R008\">Total Synthesis of a Marine Eicosanoid<\/h2>\n<figure class=\"center\"><img decoding=\"async\" src=\"\/ohmorilab\/wp-content\/themes\/org-synth\/image\/total-synth-e\/eicosanoid.png\" alt=\"\" \/><\/figure>\n<h2 id=\"R009\">Total Synthesis of Methylerysodienone<\/h2>\n<figure class=\"center\"><img decoding=\"async\" src=\"\/ohmorilab\/wp-content\/themes\/org-synth\/image\/total-synth-e\/methylerysodienone.png\" alt=\"\" \/><\/figure>\n<h2 id=\"R010\">Total Synthesis of Procyanidin<\/h2>\n<figure class=\"center\"><img decoding=\"async\" src=\"\/ohmorilab\/wp-content\/themes\/org-synth\/image\/total-synth-e\/procyanidin.png\" alt=\"\" \/><\/figure>\n<h2 id=\"R011\">Total Synthesis of Lotthanongine<\/h2>\n<figure class=\"center\"><img decoding=\"async\" src=\"\/ohmorilab\/wp-content\/themes\/org-synth\/image\/total-synth-e\/lotthanongine.png\" alt=\"\" \/><\/figure>\n<h2 id=\"R012\">Total Synthesis of Malyngolide<\/h2>\n<figure class=\"center\"><img decoding=\"async\" src=\"\/ohmorilab\/wp-content\/themes\/org-synth\/image\/total-synth-e\/malyngolide.png\" alt=\"\" \/><\/figure>\n<h2 id=\"R013\">Total Synthesis of Seragakinone A<\/h2>\n<figure class=\"center\"><img decoding=\"async\" src=\"\/ohmorilab\/wp-content\/themes\/org-synth\/image\/total-synth-e\/seragakinone.png\" alt=\"\" \/><\/figure>\n<p>[212] A. Takada, Y. Hashimoto, K. Hikita, H. Takikawa, and K. Suzuki. <em>Angew<\/em>. <em>Chem<\/em>. <em>Int<\/em>. <em>Ed<\/em>. <strong>2011<\/strong>, <em>50<\/em>, 2297.<\/p>\n<h2 id=\"R014\">Total Synthesis of BE-43472B<\/h2>\n<figure class=\"center\"><img decoding=\"async\" src=\"\/ohmorilab\/wp-content\/themes\/org-synth\/image\/total-synth-e\/BE43472B.png\" alt=\"\" \/><\/figure>\n<p>[232] Y. Yamashita, Y. Hirano, A. Takada, H. Takikawa, K. Suzuki. <em>Angew<\/em>. <em>Chem<\/em>. <em>Int<\/em>. <em>Ed<\/em>. <strong>2013<\/strong>, <em>52<\/em>, 6658.<\/p>\n<h2 id=\"R015\">Total Synthesis of Saptomycin B<\/h2>\n<figure class=\"center\"><img decoding=\"async\" src=\"\/ohmorilab\/wp-content\/themes\/org-synth\/image\/total-synth-e\/saptomycinB.png\" alt=\"\" \/><\/figure>\n<h2 id=\"R016\">Total Synthesis of Cavicularin<\/h2>\n<figure class=\"center\"><img decoding=\"async\" src=\"\/ohmorilab\/wp-content\/themes\/org-synth\/image\/total-synth-e\/cavicularin.png\" alt=\"\" \/><\/figure>\n<p>[233] H. Takiguchi, K. Ohmori, K. Suzuki, <em>Angew<\/em>. <em>Chem<\/em>. <em>Int<\/em>. <em>Ed<\/em>. <strong>2013<\/strong>, <em>52<\/em>, 10472.<\/p>\n<h2 id=\"R017\">Total Synthesis of Cinnamtannin B1<\/h2>\n<figure class=\"center\"><img decoding=\"async\" src=\"\/ohmorilab\/wp-content\/themes\/org-synth\/image\/total-synth-e\/cinnamtanninB1.png\" alt=\"\" \/><\/figure>\n<p>[237] Y. Ito, K. Ohmori, K. Suzuki, <em>Angew<\/em>. <em>Chem<\/em>. <em>Int<\/em>. <em>Ed<\/em>. <strong>2014<\/strong>, <em>53<\/em>, 10129.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Out lines for total syntheses mycinamicinIV vineomycinone B2 aquayamycin avenaciolide fraquinocins galtamycino [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"page-e.php","meta":{"_exactmetrics_skip_tracking":false,"_exactmetrics_sitenote_active":false,"_exactmetrics_sitenote_note":"","_exactmetrics_sitenote_category":0,"footnotes":""},"class_list":["post-418","page","type-page","status-publish","hentry"],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/index.php?rest_route=\/wp\/v2\/pages\/418","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=418"}],"version-history":[{"count":14,"href":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/index.php?rest_route=\/wp\/v2\/pages\/418\/revisions"}],"predecessor-version":[{"id":495,"href":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/index.php?rest_route=\/wp\/v2\/pages\/418\/revisions\/495"}],"wp:attachment":[{"href":"https:\/\/www.org-synth.chem.sci.titech.ac.jp\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=418"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}