{"id":1799,"date":"2016-11-07T13:55:40","date_gmt":"2016-11-07T13:55:40","guid":{"rendered":"http:\/\/qu.edu.iq\/repository\/?p=1799"},"modified":"2016-11-07T13:55:40","modified_gmt":"2016-11-07T13:55:40","slug":"%d8%a3-%d8%af-%d9%86%d8%a8%d9%8a%d9%84-%d8%b9%d8%a8%d8%af-%d8%b9%d8%a8%d8%af%d8%a7%d9%84%d8%b1%d8%b6%d8%a7","status":"publish","type":"post","link":"https:\/\/repository.qu.edu.iq\/?p=1799","title":{"rendered":"\u0623.\u062f.\u0646\u0628\u064a\u0644 \u0639\u0628\u062f \u0639\u0628\u062f\u0627\u0644\u0631\u0636\u0627"},"content":{"rendered":"<p style=\"text-align: left\"><a href=\"https:\/\/repository.qu.edu.iq\/wp-content\/uploads\/sites\/31\/2016\/11\/Exploration-of-new-3\u03b1\u2010pregnenolone-ester-analogues-via-Mitsunobu-reaction-1.pdf\">Exploration of new 3\u03b1\u2010pregnenolone ester analogues via Mitsunobu reaction<\/a><\/p>\n<p style=\"text-align: left\"><a href=\"https:\/\/repository.qu.edu.iq\/wp-content\/uploads\/sites\/31\/2016\/11\/Synthesis-and-characterization-of-some-new-thioxanthone-derivatives.pdf\">Synthesis and characterization of some new thioxanthone derivatives<\/a><\/p>\n<p style=\"text-align: left\"><a href=\"https:\/\/repository.qu.edu.iq\/wp-content\/uploads\/sites\/31\/2016\/11\/Synthesis-and-CYP17\u03b1-hydroxylase.pdf\">Synthesis and CYP17\u03b1 hydroxylase<\/a><\/p>\n<p style=\"text-align: left\"><a href=\"https:\/\/repository.qu.edu.iq\/wp-content\/uploads\/sites\/31\/2016\/11\/Synthesis-of-Potential-Pyrimidine.pdf\">Synthesis of Potential Pyrimidine<\/a><\/p>\n<p style=\"text-align: left\"><a href=\"https:\/\/repository.qu.edu.iq\/wp-content\/uploads\/sites\/31\/2016\/11\/Synthesis-of-Some-Substituted-Pyrimidines-Derived-from-3-Acetyl-Coumarin.pdf\">Synthesis of Some Substituted Pyrimidines Derived from 3-Acetyl Coumarin<\/a><\/p>\n<p style=\"text-align: left\"><a href=\"https:\/\/repository.qu.edu.iq\/wp-content\/uploads\/sites\/31\/2016\/11\/Synthesis-characterization-physical-and-biological-properties-of.pdf\">Synthesis, characterization, physical and biological properties of\u00a0some cholesterol derivatives<\/a><\/p>\n<p style=\"text-align: left\"><a href=\"https:\/\/repository.qu.edu.iq\/wp-content\/uploads\/sites\/31\/2016\/11\/Copper-I-catalyzed-synthesis-and-biological-evaluation-of-tetra-kis-123-tri-azoles-based-on-D-iditol-1.pdf\" target=\"_blank\" rel=\"noopener\">Copper-I-catalyzed-synthesis-and-biological-evaluation-of-tetra-kis-123-tri-azoles-based-on-D-iditol<\/a><\/p>\n<p style=\"text-align: left\"><a href=\"https:\/\/repository.qu.edu.iq\/wp-content\/uploads\/sites\/31\/2016\/11\/Copper-I-catalyzed-synthesis-and-biological-evaluation-of-tetra-kis-123-tri-azoles-based-on-D-iditol-1.pdf\" target=\"_blank\" rel=\"noopener\">Determination-of-phenolic-compounds-in-Al-Diwaniya-river-and-degradation-these-compounds-via-heterogeneous-photocatalytic-process-using-TIO2-suspension<\/a><\/p>\n<p style=\"text-align: left\"><a href=\"https:\/\/repository.qu.edu.iq\/wp-content\/uploads\/sites\/31\/2016\/11\/Generation-of-photocurrent-using-rhodamine-B-dye-and-visible-light-1.pdf\" target=\"_blank\" rel=\"noopener\">Generation-of-photocurrent-using-rhodamine-B-dye-and-visible-light<\/a><\/p>\n<p style=\"text-align: left\"><a href=\"https:\/\/repository.qu.edu.iq\/wp-content\/uploads\/sites\/31\/2016\/11\/New-biaryl-chalcone-derivative-of-pregnenolone-via-Suzuki-Miyaura-cross-coupling-reaction.-Synthesis-CYP17-hydroxylase-inhibition-activity-QSAR-and-molecular-docking-study-1.pdf\" target=\"_blank\" rel=\"noopener\">New-biaryl-chalcone-derivative-of-pregnenolone-via-Suzuki-Miyaura-cross-coupling-reaction.-Synthesis-CYP17-hydroxylase-inhibition-activity-QSAR-and-molecular-docking-study<\/a><\/p>\n<p style=\"text-align: left\"><a href=\"https:\/\/repository.qu.edu.iq\/wp-content\/uploads\/sites\/31\/2016\/11\/Preparation-of-Glycoside-Compounds-Containing-of-Different-Cyclic-Substituents-1.pdf\" target=\"_blank\" rel=\"noopener\">Preparation-of-Glycoside-Compounds-Containing-of-Different-Cyclic-Substituents<\/a><\/p>\n<p style=\"text-align: left\"><a href=\"https:\/\/repository.qu.edu.iq\/wp-content\/uploads\/sites\/31\/2016\/11\/Study-the-efficiency-of-thermal-conversion-of-some-organic-dyes-in-aqueous-solution-2.pdf\" target=\"_blank\" rel=\"noopener\">Study-the-efficiency-of-thermal-conversion-of-some-organic-dyes-in-aqueous-solution<\/a><\/p>\n<p style=\"text-align: left\"><a href=\"https:\/\/repository.qu.edu.iq\/wp-content\/uploads\/sites\/31\/2016\/11\/symthesis-and-CYP17-alfa-hydroxylase-inhibition-activty-of-new-3alfa-and-3beta-ester-derivatives-of-pregnenolone-and-related-ether-analogues-1.pdf\" target=\"_blank\" rel=\"noopener\">symthesis-and-CYP17-alfa-hydroxylase-inhibition-activty-of-new-3alfa-and-3beta-ester-derivatives-of-pregnenolone-and-related-ether-analogues<\/a><\/p>\n<p style=\"text-align: left\"><a href=\"https:\/\/repository.qu.edu.iq\/wp-content\/uploads\/sites\/31\/2016\/11\/symthesis-and-CYP17-alfa-hydroxylase-inhibition-activty-of-new-3alfa-and-3beta-ester-derivatives-of-pregnenolone-and-related-ether-analogues-1.pdf\" target=\"_blank\" rel=\"noopener\">Synthesis-of-new-Schiff-Bases-via-Suzuki-coupling-reaction<\/a><\/p>\n<p style=\"text-align: left\"><a href=\"https:\/\/repository.qu.edu.iq\/wp-content\/uploads\/sites\/31\/2016\/11\/Determination-of-phenolic-compounds-in-Al-Diwaniya-river-and-degradation-these-compounds-via-heterogeneous-photocatalytic-process-using-TIO2-suspension-1.pdf\" target=\"_blank\" rel=\"noopener\">synthesis-of-substituted-pyrimidines-derived-from-3-acetyl-coumarin<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Exploration of new 3\u03b1\u2010pregnenolone ester analogues via Mitsunobu reaction Synthesis and characterization of some new thioxanthone derivatives Synthesis and CYP17\u03b1 &#8230; <a class=\"cz_readmore\" href=\"https:\/\/repository.qu.edu.iq\/?p=1799\"><i class=\"fa fa-sign-out\" aria-hidden=\"true\"><\/i><span>\u0642\u0631\u0627\u0621\u0629 \u0627\u0644\u0645\u0632\u064a\u062f<\/span><\/a><\/p>\n","protected":false},"author":74,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[3],"tags":[],"class_list":["post-1799","post","type-post","status-publish","format-standard","hentry","category-uncategorized"],"_links":{"self":[{"href":"https:\/\/repository.qu.edu.iq\/index.php?rest_route=\/wp\/v2\/posts\/1799","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/repository.qu.edu.iq\/index.php?rest_route=\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/repository.qu.edu.iq\/index.php?rest_route=\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/repository.qu.edu.iq\/index.php?rest_route=\/wp\/v2\/users\/74"}],"replies":[{"embeddable":true,"href":"https:\/\/repository.qu.edu.iq\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=1799"}],"version-history":[{"count":0,"href":"https:\/\/repository.qu.edu.iq\/index.php?rest_route=\/wp\/v2\/posts\/1799\/revisions"}],"wp:attachment":[{"href":"https:\/\/repository.qu.edu.iq\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=1799"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/repository.qu.edu.iq\/index.php?rest_route=%2Fwp%2Fv2%2Fcategories&post=1799"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/repository.qu.edu.iq\/index.php?rest_route=%2Fwp%2Fv2%2Ftags&post=1799"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}