{"@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/1360004232524828672.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1016/j.tet.2011.05.107"}},{"identifier":{"@type":"URI","@value":"https://api.elsevier.com/content/article/PII:S0040402011007976?httpAccept=text/xml"}},{"identifier":{"@type":"URI","@value":"https://api.elsevier.com/content/article/PII:S0040402011007976?httpAccept=text/plain"}}],"resourceType":"学術雑誌論文(journal article)","dc:title":[{"@value":"Ten new fawcettimine-related alkaloids from three species of Lycopodium"}],"description":[{"notation":[{"@value":"Abstract   Ten new fawcettimine-related alkaloids, i.e., lycopoclavamines, lycoposquarrosamine-A, and other hydroxylated fawcettimine derivatives, were isolated from three species of  Lycopodium  ( Lycopodium clavatum ,  Lycopodium serratum ,  and Lycopodium squarrosum ). The structures of the new alkaloids were elucidated by spectroscopic methods and chemical correlation."}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1420001326237216384","@type":"Researcher","personIdentifier":[{"@type":"KAKEN_RESEARCHERS","@value":"90433606"},{"@type":"NRID","@value":"1000090433606"},{"@type":"NRID","@value":"9000409025883"},{"@type":"NRID","@value":"9000398838284"},{"@type":"NRID","@value":"9000396141921"},{"@type":"NRID","@value":"9000243895308"},{"@type":"NRID","@value":"9000005136504"},{"@type":"NRID","@value":"9000375901318"},{"@type":"NRID","@value":"9000006709566"},{"@type":"NRID","@value":"9000264273104"},{"@type":"NRID","@value":"9000259830846"},{"@type":"NRID","@value":"9000272641937"},{"@type":"NRID","@value":"9000396146700"},{"@type":"RESEARCHMAP","@value":"https://researchmap.jp/katakawa"}],"foaf:name":[{"@value":"Kazuaki Katakawa"}]},{"@id":"https://cir.nii.ac.jp/crid/1380004232524828678","@type":"Researcher","foaf:name":[{"@value":"Hiroko Mito"}]},{"@id":"https://cir.nii.ac.jp/crid/1420845751166164096","@type":"Researcher","personIdentifier":[{"@type":"KAKEN_RESEARCHERS","@value":"80396689"},{"@type":"NRID","@value":"1000080396689"},{"@type":"NRID","@value":"9000005136679"},{"@type":"NRID","@value":"9000264273063"},{"@type":"NRID","@value":"9000391974206"},{"@type":"NRID","@value":"9000356653609"},{"@type":"NRID","@value":"9000006710022"},{"@type":"NRID","@value":"9000010700930"},{"@type":"NRID","@value":"9000391963183"},{"@type":"NRID","@value":"9000391970652"},{"@type":"NRID","@value":"9000326650750"},{"@type":"NRID","@value":"9000396141196"},{"@type":"NRID","@value":"9000018499412"},{"@type":"NRID","@value":"9000020407033"},{"@type":"NRID","@value":"9000389944309"},{"@type":"NRID","@value":"9000398278573"},{"@type":"NRID","@value":"9000403024130"},{"@type":"NRID","@value":"9000403045725"},{"@type":"NRID","@value":"9000411532871"},{"@type":"NRID","@value":"9000383838402"},{"@type":"NRID","@value":"9000019012213"},{"@type":"NRID","@value":"9000019946420"},{"@type":"NRID","@value":"9000391963324"},{"@type":"NRID","@value":"9000010672079"},{"@type":"NRID","@value":"9000415154301"},{"@type":"NRID","@value":"9000399572874"},{"@type":"RESEARCHMAP","@value":"https://researchmap.jp/noriyuki-kogure"}],"foaf:name":[{"@value":"Noriyuki Kogure"}]},{"@id":"https://cir.nii.ac.jp/crid/1380004232524828675","@type":"Researcher","foaf:name":[{"@value":"Mariko Kitajima"}]},{"@id":"https://cir.nii.ac.jp/crid/1380004232524828673","@type":"Researcher","foaf:name":[{"@value":"Sumphan Wongseripipatana"}]},{"@id":"https://cir.nii.ac.jp/crid/1380004232524828672","@type":"Researcher","foaf:name":[{"@value":"Munehisa Arisawa"}]},{"@id":"https://cir.nii.ac.jp/crid/1380004232524828674","@type":"Researcher","foaf:name":[{"@value":"Hiromitsu Takayama"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"00404020"}],"prism:publicationName":[{"@value":"Tetrahedron"}],"dc:publisher":[{"@value":"Elsevier BV"}],"prism:publicationDate":"2011-09","prism:volume":"67","prism:number":"35","prism:startingPage":"6561","prism:endingPage":"6567"},"reviewed":"false","dc:rights":["https://www.elsevier.com/tdm/userlicense/1.0/","https://www.elsevier.com/legal/tdmrep-license"],"url":[{"@id":"https://api.elsevier.com/content/article/PII:S0040402011007976?httpAccept=text/xml"},{"@id":"https://api.elsevier.com/content/article/PII:S0040402011007976?httpAccept=text/plain"}],"createdAt":"2011-06-05","modifiedAt":"2025-09-22","project":[{"@id":"https://cir.nii.ac.jp/crid/1040000782112139904","@type":"Project","projectIdentifier":[{"@type":"KAKEN","@value":"22390019"},{"@type":"JGN","@value":"JP22390019"},{"@type":"URI","@value":"https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-22390019/"}],"notation":[{"@language":"ja","@value":"脳機能障害と痛みを制御する機能性天然分子の探索・合成と創薬研究への展開"},{"@language":"en","@value":"Studies on isolation, total synthesis and medicinal chemistryof natural products with regulating activities on memory and pain."}]},{"@id":"https://cir.nii.ac.jp/crid/1040282257161456512","@type":"Project","projectIdentifier":[{"@type":"KAKEN","@value":"23790124"},{"@type":"JGN","@value":"JP23790124"},{"@type":"URI","@value":"https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-23790124/"}],"notation":[{"@language":"ja","@value":"AChE阻害活性を有する植物アルカロイドの探索・全合成と構造活性相関の検討"},{"@language":"en","@value":"Studies on isolation, total syntheses and structure-activity relationship of plants alkaloids with AChE inhibitory activity"}]}],"relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1360004229991186816","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Redox Divergent Synthesis of Fawcettimine‐Type <i>Lycopodium</i> Alkaloids"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285707501795584","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"β-Carboline-type indole alkaloid glycosides from Ophiorrhiza trichocarpon"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285708108280192","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Asymmetric Total Synthesis of Fawcettimine-Type <i>Lycopodium</i> Alkaloid, Lycopoclavamine-A"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292619931554048","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Enantiospecific Formal Total Synthesis of (+)-Fawcettimine"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292620417879552","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Lycoflexine, a new type of lycopodium alkaloid"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567182478631168","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total synthesis of (±)-lycoposerramine-R, a novel skeletal type of  Lycopodium alkaloid"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567182481557248","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Concise asymmetric total synthesis of lycopodine and flabelliformine via cascade cyclization reaction"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567183202981248","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Syntheses of (±)-Serratine, (±)-Lycoposerramine T, and (±)-Lycopoclavamine B"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574093757935104","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The Lycopodium Alkaloids"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574096325894016","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Seven new Lycopodium alkaloids, lycoposerramines-C, -D, -E, -P, -Q, -S, and -U, from Lycopodium serratum Thunb."}]},{"@id":"https://cir.nii.ac.jp/crid/1360848657457486976","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Chemical conversion of strychnine into kopsiyunnanine-I, a new hexacyclic indole alkaloid from Yunnan Kopsia arborea"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848658527974784","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"The first asymmetric total synthesis of lycoposerramine-R"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855569510845696","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A divergent approach for the total syntheses of cernuane-type and quinolizidine-type Lycopodium alkaloids"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418520712751104","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Asymmetric Total Syntheses of Cyclic Nitrone-Containing Phlegmarine-Type <i>Lycopodium</i> Alkaloids, Lycoposerramines-X and -Z"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699995375938048","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"First Asymmetric Total Syntheses of Cernuane-Type Lycopodium Alkaloids, Cernuine, and Cermizine D"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699995696148864","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Lycopodium Alkaloids: Isolation and Asymmetric Synthesis"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981471108621312","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Fawcettimine-Related Alkaloids from <i>Lycopodium </i><i>serratum</i>"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981471232089856","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"First Asymmetric Total Syntheses of Fawcettimine-Type <i>Lycopodium</i> Alkaloids, Lycoposerramine-C and Phlegmariurine-A"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262943953048192","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Three New Phlegmarine-Type Lycopodium Alkaloids, Lycoposerramines-X, -Y and -Z, Having a Nitrone Residue, from Lycopodium serratum"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262944149254272","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The Lycopodium alkaloids"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262944689390720","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Lycovatine A, a C16N-Type Quaternary Alkaloid from Lycopodium clavatum var. robustum"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825893759613696","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A New <i>Lycopodium</i> Alkaloid, Lycoposerramine‐R, with a Novel Skeleton and Three New Fawcettimine‐Related Alkaloids from <i>Lycopodium serratum</i>"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825894514842496","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of the Lycopodium Alkaloid (+)-Lycoflexine"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107370399013760","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The effects of huperzine A and IDRA 21 on visual recognition memory in young macaques"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951795643652224","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Asymmetric Total Syntheses of Two Phlegmarine-Type Alkaloids, Lycoposerramines-V and -W, Newly Isolated from<i>Lycopodium serratum</i>"}]},{"@id":"https://cir.nii.ac.jp/crid/1390001204167231744","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@language":"en","@value":"The structures of two lycopodium alkaloids, lycothunine and lycophlegmarine, and the configuration of the C3-C4 bond of fawcettimine and fawcettidine."}]},{"@id":"https://cir.nii.ac.jp/crid/1390282679154112256","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"New Lycopodine-Type Alkaloids from <i>Lycopodium carinatum</i>"},{"@value":"New Lycopodine-Type Alkaloids from Lycopodium carinatum"}]},{"@id":"https://cir.nii.ac.jp/crid/1390282679154279808","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"New Alkaloids from <i>Lycopodium japonicum</i>"},{"@value":"New Alkaloids from Lycopodium japonicum"}]},{"@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":"10.1016/j.tet.2011.05.107"},{"@type":"KAKEN","@value":"PRODUCT-13348295"},{"@type":"KAKEN","@value":"PRODUCT-13348345"},{"@type":"KAKEN","@value":"PRODUCT-14403692"},{"@type":"OPENAIRE","@value":"doi_dedup___::1a39314715b302102ea1daad9c565487"},{"@type":"CROSSREF","@value":"10.1002/chem.201403163_references_DOI_DofdUtD3ru1TmVf9XJFdrB7n9es"},{"@type":"CROSSREF","@value":"10.1016/j.tetlet.2018.12.007_references_DOI_DofdUtD3ru1TmVf9XJFdrB7n9es"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20220049_references_DOI_DofdUtD3ru1TmVf9XJFdrB7n9es"},{"@type":"CROSSREF","@value":"10.1016/j.tet.2014.11.038_references_DOI_DofdUtD3ru1TmVf9XJFdrB7n9es"},{"@type":"CROSSREF","@value":"10.1039/c5ob00827a_references_DOI_DofdUtD3ru1TmVf9XJFdrB7n9es"},{"@type":"CROSSREF","@value":"10.1016/j.tet.2013.08.070_references_DOI_DofdUtD3ru1TmVf9XJFdrB7n9es"},{"@type":"CROSSREF","@value":"10.1021/acs.joc.9b00586_references_DOI_DofdUtD3ru1TmVf9XJFdrB7n9es"},{"@type":"CROSSREF","@value":"10.1248/cpb.c12-00201_references_DOI_DofdUtD3ru1TmVf9XJFdrB7n9es"},{"@type":"CROSSREF","@value":"10.1016/j.tetlet.2012.09.078_references_DOI_DofdUtD3ru1TmVf9XJFdrB7n9es"},{"@type":"CROSSREF","@value":"10.1021/ol400628h_references_DOI_DofdUtD3ru1TmVf9XJFdrB7n9es"},{"@type":"CROSSREF","@value":"10.1248/cpb.c16-00171_references_DOI_DofdUtD3ru1TmVf9XJFdrB7n9es"}]}