{"id":{"repo_id":"edinburgh","oai_identifier":"oai:era.ed.ac.uk:1842/34405"},"canonical_url":"https://search.dev.ndltd.org/etd/edinburgh/oai:era.ed.ac.uk:1842/34405","repository":{"repo_id":"edinburgh","name":"University of Edinburgh","base_url":"https://era.ed.ac.uk/server/oai/request"},"display":{"title":"A comparison of some of the ergot alkaloids","abstract":"The ergot alkaloids, other than those that are molecular compounds, fail into two groups, a laevorotatory physiologically active group, and a dextrorotatory group which is considerably less active. Smith and Timmis drew attention to this fact in their paper on isoergine and isolysergic acids (1).","abstract_html":"The ergot alkaloids, other than those that are molecular compounds, fail into two groups, a laevorotatory physiologically active group, and a dextrorotatory group which is considerably less active. Smith and Timmis drew attention to this fact in their paper on isoergine and isolysergic acids (1).","abstract_has_math":false,"creators":["White, Adam Cairns"],"institution":"The University of Edinburgh","degree_name":null,"degree_level":null,"degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":1939,"date_issued":"1939","date_published":"1939","updated_at":"2026-07-24T02:14:22Z","subjects":[],"languages":[],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/1842/34405","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:creator","label":"Author","values":["White, Adam Cairns"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2019-02-15T14:26:38Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2019-02-15T14:26:38Z"]},{"key":"dc:date.issued","label":"Date","values":["1939"]},{"key":"dc:publisher","label":"Institution","values":["The University of Edinburgh"]},{"key":"dc:type","label":"Dc Type","values":["Thesis or Dissertation"]},{"key":"dc:type.qualificationlevel","label":"Dc Type Qualificationlevel","values":["Doctoral"]},{"key":"dc:type.qualificationname","label":"Dc Type Qualificationname","values":["MD Doctor of Medicine"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["http://hdl.handle.net/1842/34405"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["The ergot alkaloids, other than those that are molecular compounds, fail into two groups, a laevorotatory physiologically active group, and a dextrorotatory group which is considerably less active. Smith and Timmis drew attention to this fact in their paper on isoergine and isolysergic acids (1).","In Table l I have assembled the ergot alkaloids in descending order of the number of constituent carbon atoms, and given, where possible, their rotations in chloroform. The figures are obtained from the papers of Smith and Timmis (1) (2). The decomposition products, ergine and isoergine have also been included."]},{"key":"dc:title","label":"Title","values":["A comparison of some of the ergot alkaloids"]}]}],"canonical_facts":{"dc:creator":["White, Adam Cairns"],"dc:date.accessioned":["2019-02-15T14:26:38Z"],"dc:date.available":["2019-02-15T14:26:38Z"],"dc:date.issued":["1939"],"dc:description.abstract":["The ergot alkaloids, other than those that are molecular compounds, fail into two groups, a laevorotatory physiologically active group, and a dextrorotatory group which is considerably less active. Smith and Timmis drew attention to this fact in their paper on isoergine and isolysergic acids (1).","In Table l I have assembled the ergot alkaloids in descending order of the number of constituent carbon atoms, and given, where possible, their rotations in chloroform. The figures are obtained from the papers of Smith and Timmis (1) (2). The decomposition products, ergine and isoergine have also been included."],"dc:identifier.uri":["http://hdl.handle.net/1842/34405"],"dc:publisher":["The University of Edinburgh"],"dc:title":["A comparison of some of the ergot alkaloids"],"dc:type":["Thesis or Dissertation"],"dc:type.qualificationlevel":["Doctoral"],"dc:type.qualificationname":["MD Doctor of Medicine"]},"updated_at":"2026-07-24T02:14:22Z"}