{"id":{"repo_id":"uab","oai_identifier":"oai:digitalcommons.library.uab.edu:etd-collection-8039"},"canonical_url":"https://search.dev.ndltd.org/etd/uab/oai:digitalcommons.library.uab.edu:etd-collection-8039","repository":{"repo_id":"uab","name":"University of Alabama Birmingham","base_url":"https://digitalcommons.library.uab.edu/do/oai/"},"display":{"title":"The Reactions of Ethyl Ethoxymagnesiomalonate With Some Simple Aliphatic Diacid Chlorides.","abstract":"Due to the biochemical and pharmacological interest in cyclitols, alone, and in combination with other molecules, the biosynthesis of these compounds has been studied in a number of laboratories. Kiely and Sherman recently developed a chemical model which describes the proposed mechanism for the cyclization step in the biosynthesis of the most common cyclitol, myo-inositol.","abstract_html":"Due to the biochemical and pharmacological interest in cyclitols, alone, and in combination with other molecules, the biosynthesis of these compounds has been studied in a number of laboratories. Kiely and Sherman recently developed a chemical model which describes the proposed mechanism for the cyclization step in the biosynthesis of the most common cyclitol, myo-inositol.","abstract_has_math":false,"creators":["Nix, Collier B"],"institution":null,"degree_name":null,"degree_level":"Thesis","degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":1977,"date_issued":"1977-01-01T08:00:00Z","date_published":"1977-01-01T08:00:00Z","updated_at":"2026-07-24T05:05:51Z","subjects":["Biosynthesis","Ethoxymagnesiomalonate","Cyclitols","Delta dicarbonyl sugars"],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"https://digitalcommons.library.uab.edu/etd-collection/7047","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:creator","label":"Author","values":["Nix, Collier B"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"thesis:degree_level","label":"Degree Level","values":["Thesis"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Biosynthesis","Ethoxymagnesiomalonate","Cyclitols","Delta dicarbonyl sugars"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["https://digitalcommons.library.uab.edu/etd-collection/7047"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Due to the biochemical and pharmacological interest in cyclitols, alone, and in combination with other molecules, the biosynthesis of these compounds has been studied in a number of laboratories. Kiely and Sherman recently developed a chemical model which describes the proposed mechanism for the cyclization step in the biosynthesis of the most common cyclitol, myo-inositol."]},{"key":"dc:title","label":"Title","values":["The Reactions of Ethyl Ethoxymagnesiomalonate With Some Simple Aliphatic Diacid Chlorides."]}]}],"canonical_facts":{"dc:creator":["Nix, Collier B"],"dc:description.abstract":["Due to the biochemical and pharmacological interest in cyclitols, alone, and in combination with other molecules, the biosynthesis of these compounds has been studied in a number of laboratories. Kiely and Sherman recently developed a chemical model which describes the proposed mechanism for the cyclization step in the biosynthesis of the most common cyclitol, myo-inositol."],"dc:identifier":["https://digitalcommons.library.uab.edu/etd-collection/7047"],"dc:subject":["Biosynthesis","Ethoxymagnesiomalonate","Cyclitols","Delta dicarbonyl sugars"],"dc:title":["The Reactions of Ethyl Ethoxymagnesiomalonate With Some Simple Aliphatic Diacid Chlorides."],"thesis:degree_level":["Thesis"]},"updated_at":"2026-07-24T05:05:51Z"}