{"id":{"repo_id":"creighton","oai_identifier":"oai:cdr.creighton.edu:10504/109109"},"canonical_url":"https://search.dev.ndltd.org/etd/creighton/oai:cdr.creighton.edu:10504/109109","repository":{"repo_id":"creighton","name":"Creighton University","base_url":"https://cdr.creighton.edu/server/oai/request"},"display":{"title":"The Synthesis of 5-[(P-Hydroxyphenyl)-2, 4, 6-Tricarbethoxy]-Cyclohexanedione-1, 3.","abstract":"Papadakis has described the synthesis of (p-hydroxyphenyl)-cyclohexanedione-l, 3 via 5-[(p- acetoxyphenyl)-4, 6-dicarbethoxy]-cyclohexanedione-1, 3 as shown in equations 1-8 of the flow sheet. |The structures of these compounds are such that they can serve as intermediates for the preparation of compounds resembling steriods. They have functional groups which can afford alkylation, acylation, Grignard, Reformatsky, halogenation, and many other type reactions.","abstract_html":"Papadakis has described the synthesis of (p-hydroxyphenyl)-cyclohexanedione-l, 3 via 5-[(p- acetoxyphenyl)-4, 6-dicarbethoxy]-cyclohexanedione-1, 3 as shown in equations 1-8 of the flow sheet. |The structures of these compounds are such that they can serve as intermediates for the preparation of compounds resembling steriods. They have functional groups which can afford alkylation, acylation, Grignard, Reformatsky, halogenation, and many other type reactions.","abstract_has_math":false,"creators":["Johnson, Bernard Dean"],"institution":"Creighton University","degree_name":null,"degree_level":null,"degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":["Papadakis, Phillippos E."],"committee_chairs":[],"committee_members":[],"year":1962,"date_issued":"1962","date_published":"1962","updated_at":"2026-07-24T01:51:52Z","subjects":[],"languages":["en_US"],"rights":["A non-exclusive distribution right is granted to Creighton University and to ProQuest following the publishing model selected above."],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/10504/109109","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Papadakis, Phillippos E."]},{"key":"dc:creator","label":"Author","values":["Johnson, Bernard Dean"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2017-01-24T18:54:44Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2017-01-24T18:54:44Z"]},{"key":"dc:date.issued","label":"Date","values":["1962"]},{"key":"dc:publisher","label":"Institution","values":["Creighton University"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language.iso","label":"Language (ISO)","values":["en_US"]},{"key":"dc:rights","label":"Dc Rights","values":["A non-exclusive distribution right is granted to Creighton University and to ProQuest following the publishing model selected above."]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["http://hdl.handle.net/10504/109109"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Papadakis has described the synthesis of (p-hydroxyphenyl)-cyclohexanedione-l, 3 via 5-[(p- acetoxyphenyl)-4, 6-dicarbethoxy]-cyclohexanedione-1, 3 as shown in equations 1-8 of the flow sheet. |The structures of these compounds are such that they can serve as intermediates for the preparation of compounds resembling steriods. They have functional groups which can afford alkylation, acylation, Grignard, Reformatsky, halogenation, and many other type reactions."]},{"key":"dc:title","label":"Title","values":["The Synthesis of 5-[(P-Hydroxyphenyl)-2, 4, 6-Tricarbethoxy]-Cyclohexanedione-1, 3."]}]}],"canonical_facts":{"dc:contributor.advisor":["Papadakis, Phillippos E."],"dc:creator":["Johnson, Bernard Dean"],"dc:date.accessioned":["2017-01-24T18:54:44Z"],"dc:date.available":["2017-01-24T18:54:44Z"],"dc:date.issued":["1962"],"dc:description.abstract":["Papadakis has described the synthesis of (p-hydroxyphenyl)-cyclohexanedione-l, 3 via 5-[(p- acetoxyphenyl)-4, 6-dicarbethoxy]-cyclohexanedione-1, 3 as shown in equations 1-8 of the flow sheet. |The structures of these compounds are such that they can serve as intermediates for the preparation of compounds resembling steriods. They have functional groups which can afford alkylation, acylation, Grignard, Reformatsky, halogenation, and many other type reactions."],"dc:identifier.uri":["http://hdl.handle.net/10504/109109"],"dc:language.iso":["en_US"],"dc:publisher":["Creighton University"],"dc:rights":["A non-exclusive distribution right is granted to Creighton University and to ProQuest following the publishing model selected above."],"dc:title":["The Synthesis of 5-[(P-Hydroxyphenyl)-2, 4, 6-Tricarbethoxy]-Cyclohexanedione-1, 3."],"dc:type":["Thesis"]},"updated_at":"2026-07-24T01:51:52Z"}