{"id":183,"date":"2016-07-07T16:59:42","date_gmt":"2016-07-07T20:59:42","guid":{"rendered":"https:\/\/sites.berry.edu\/mturlington\/?page_id=183"},"modified":"2018-06-14T10:55:29","modified_gmt":"2018-06-14T14:55:29","slug":"harrison-hill","status":"publish","type":"page","link":"https:\/\/sites.berry.edu\/mturlington\/group-members\/harrison-hill\/","title":{"rendered":"Harrison Hill"},"content":{"rendered":"<p><img loading=\"lazy\" decoding=\"async\" class=\"size-medium wp-image-185 alignleft\" src=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2016\/07\/IMG_2951-300x200.jpg\" alt=\"IMG_1015\" width=\"300\" height=\"200\" \/><\/p>\n<p><strong>Major<\/strong>: \u00a0Chemistry<\/p>\n<p><strong>Class<\/strong>: \u00a02018<\/p>\n<p><strong>Research Projects<\/strong>: Enantioselective Synthesis of Aza-Heterocycles;\u00a0Stereoselective\u00a0Synthesis of Terminal Bromo-Substituted Propargylamines<\/p>\n<p><strong>Career Plans:\u00a0 <\/strong>Chemistry\u00a0Graduate<strong>\u00a0<\/strong>Student, University of Notre Dame<\/p>\n<p><strong>Publications: \u00a0\u00a0<\/strong>\u201cA flexible method for the synthesis of 2-substituted 1,2,5,6-tetrahydropyridines and piperidines from chloro-containing propargylamines.\u201d\u00a0<em>Tetrahedron Lett.\u00a0<\/em><strong>2017<\/strong>, <i>58<\/i>, 470-473.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Major: \u00a0Chemistry Class: \u00a02018 Research Projects: Enantioselective Synthesis of Aza-Heterocycles;\u00a0Stereoselective\u00a0Synthesis of Terminal Bromo-Substituted Propargylamines Career Plans:\u00a0 Chemistry\u00a0Graduate\u00a0Student, University of Notre Dame Publications: \u00a0\u00a0\u201cA flexible method for the synthesis of 2-substituted [&hellip;]<\/p>\n","protected":false},"author":77,"featured_media":0,"parent":71,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-183","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/sites.berry.edu\/mturlington\/wp-json\/wp\/v2\/pages\/183","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/sites.berry.edu\/mturlington\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/sites.berry.edu\/mturlington\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/sites.berry.edu\/mturlington\/wp-json\/wp\/v2\/users\/77"}],"replies":[{"embeddable":true,"href":"https:\/\/sites.berry.edu\/mturlington\/wp-json\/wp\/v2\/comments?post=183"}],"version-history":[{"count":7,"href":"https:\/\/sites.berry.edu\/mturlington\/wp-json\/wp\/v2\/pages\/183\/revisions"}],"predecessor-version":[{"id":485,"href":"https:\/\/sites.berry.edu\/mturlington\/wp-json\/wp\/v2\/pages\/183\/revisions\/485"}],"up":[{"embeddable":true,"href":"https:\/\/sites.berry.edu\/mturlington\/wp-json\/wp\/v2\/pages\/71"}],"wp:attachment":[{"href":"https:\/\/sites.berry.edu\/mturlington\/wp-json\/wp\/v2\/media?parent=183"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}