{"@context":{"@vocab":"https://cir.nii.ac.jp/schema/1.0/","rdfs":"http://www.w3.org/2000/01/rdf-schema#","dc":"http://purl.org/dc/elements/1.1/","dcterms":"http://purl.org/dc/terms/","foaf":"http://xmlns.com/foaf/0.1/","prism":"http://prismstandard.org/namespaces/basic/2.0/","cinii":"http://ci.nii.ac.jp/ns/1.0/","datacite":"https://schema.datacite.org/meta/kernel-4/","ndl":"http://ndl.go.jp/dcndl/terms/","jpcoar":"https://github.com/JPCOAR/schema/blob/master/2.0/"},"@id":"https://cir.nii.ac.jp/crid/1362262943937165952.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1139/v63-452"}},{"identifier":{"@type":"URI","@value":"https://cdnsciencepub.com/doi/pdf/10.1139/v63-452"}}],"dc:title":[{"@value":"LYCOPODIUM ALKALOIDS: PART VIII. NEW ALKALOIDS FROM JAMAICAN LYCOPODIUM SPECIES"}],"description":[{"type":"abstract","notation":[{"@value":"<jats:p> Four more alkaloids have been isolated from Lycopodium fawcettii. Lycodine and des-N-methyl-α-obscurine have been found in other Lycopodium species but base L, C<jats:sub>18</jats:sub>H<jats:sub>31</jats:sub>NO<jats:sub>4</jats:sub>, and base R, C<jats:sub>16</jats:sub>H<jats:sub>24</jats:sub>N<jats:sub>2</jats:sub>O<jats:sub>2</jats:sub>, are new. Some transformations of base L are described including its conversion to the previously described base O. An unstable base from L. clavatum has been characterized as the picrate C<jats:sub>15</jats:sub>H<jats:sub>25</jats:sub>NO<jats:sub>3</jats:sub>.C<jats:sub>6</jats:sub>H<jats:sub>3</jats:sub>N<jats:sub>3</jats:sub>O<jats:sub>7</jats:sub>. Further characterization of the two bases fawcettidine (base F) and fawcettimine (base A) is reported. </jats:p>"}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1382262943937165952","@type":"Researcher","foaf:name":[{"@value":"R. H. Burnell"}]},{"@id":"https://cir.nii.ac.jp/crid/1382262943937165953","@type":"Researcher","foaf:name":[{"@value":"C. G. Chin"}]},{"@id":"https://cir.nii.ac.jp/crid/1382262943937165954","@type":"Researcher","foaf:name":[{"@value":"B. S. Mootoo"}]},{"@id":"https://cir.nii.ac.jp/crid/1382262943937165955","@type":"Researcher","foaf:name":[{"@value":"D. R. Taylor"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"00084042"},{"@type":"EISSN","@value":"14803291"}],"prism:publicationName":[{"@value":"Canadian Journal of Chemistry"}],"dc:publisher":[{"@value":"Canadian Science Publishing"}],"prism:publicationDate":"1963-12-01","prism:volume":"41","prism:number":"12","prism:startingPage":"3091","prism:endingPage":"3094"},"reviewed":"false","dc:rights":["http://www.nrcresearchpress.com/page/about/CorporateTextAndDataMining"],"url":[{"@id":"https://cdnsciencepub.com/doi/pdf/10.1139/v63-452"}],"createdAt":"2006-05-02","modifiedAt":"2025-07-02","relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1050282813185877120","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Synthesis of Octahydro- and Decahydroquinolines by a One-Pot Cascade Reaction of Tetrasubstituted Enecarbamate"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285708206259328","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total Syntheses of (+)-Fawcettimine and (+)-Lycoposerramine-B"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567179943124352","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total Syntheses of (±)‐Fawcettimine, (±)‐Fawcettidine, (±)‐Lycoflexine, and (±)‐Lycoposerramine‐Q"}]},{"@id":"https://cir.nii.ac.jp/crid/2051151842062065792","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total synthesis of lyconesidine B : approach to a three-dimensional tetracyclic skeleton of amine-type fawcettimine core and studies of asymmetric synthesis"}]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1139/v63-452"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20220049_references_DOI_AAd4yzyPDjvJ2xkXSkJJlb0F5eD"},{"@type":"CROSSREF","@value":"10.1002/chem.201300364_references_DOI_AAd4yzyPDjvJ2xkXSkJJlb0F5eD"},{"@type":"CROSSREF","@value":"10.1021/jo100499h_references_DOI_AAd4yzyPDjvJ2xkXSkJJlb0F5eD"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.7b02122_references_DOI_AAd4yzyPDjvJ2xkXSkJJlb0F5eD"}]}