{"@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/1363670320546815104.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1021/ol047356q"}},{"identifier":{"@type":"URI","@value":"https://pubs.acs.org/doi/pdf/10.1021/ol047356q"}}],"dc:title":[{"@value":"Lewis Acid Assisted Ring-Closing Metathesis of Chiral Diallylamines:  An Efficient Approach to Enantiopure Pyrrolidine Derivatives"}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1383670320546815232","@type":"Researcher","foaf:name":[{"@value":"Qian Yang"}],"jpcoar:affiliationName":[{"@value":"The Key Laboratory of Pesticide and Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, 152 Luoyu Road, Wuhan, Hubei 430079, China, and Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian, Liaoning 116023, China"}]},{"@id":"https://cir.nii.ac.jp/crid/1383670320546815233","@type":"Researcher","foaf:name":[{"@value":"Wen-Jing Xiao"}],"jpcoar:affiliationName":[{"@value":"The Key Laboratory of Pesticide and Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, 152 Luoyu Road, Wuhan, Hubei 430079, China, and Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian, Liaoning 116023, China"}]},{"@id":"https://cir.nii.ac.jp/crid/1383670320546815104","@type":"Researcher","foaf:name":[{"@value":"Zhengkun Yu"}],"jpcoar:affiliationName":[{"@value":"The Key Laboratory of Pesticide and Chemical Biology, Ministry of Education, College of Chemistry, Central China Normal University, 152 Luoyu Road, Wuhan, Hubei 430079, China, and Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 457 Zhongshan Road, Dalian, Liaoning 116023, China"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"15237060"},{"@type":"EISSN","@value":"15237052"}],"prism:publicationName":[{"@value":"Organic Letters"}],"dc:publisher":[{"@value":"American Chemical Society (ACS)"}],"prism:publicationDate":"2005-01-28","prism:volume":"7","prism:number":"5","prism:startingPage":"871","prism:endingPage":"874"},"reviewed":"false","url":[{"@id":"https://pubs.acs.org/doi/pdf/10.1021/ol047356q"}],"createdAt":"2005-02-24","modifiedAt":"2021-09-19","relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1050012570394120448","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Bithiophene with Winding Vine-shaped Molecular Asymmetry. Preparation, Structural Characterization, and Enantioselective Synthesis"}]},{"@id":"https://cir.nii.ac.jp/crid/1050294045370686208","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Enantioselective Synthesis of Macrocyclic Heterobiaryl Derivatives of Molecular Asymmetry by Molybdenum-Catalyzed Asymmetric Ring-Closing Metathesis"},{"@value":"Enantioselective Synthesis of Macrocyclic Heterobiaryl Derivatives of Molecular Asymmetry by Molybdenum‐Catalyzed Asymmetric Ring‐Closing Metathesis"}]},{"@id":"https://cir.nii.ac.jp/crid/1050571948037518720","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Total Synthesis of Lyconesidine B, a Lycopodium Alkaloid with an Oxygenated, Amine-Type Fawcettimine Core"},{"@value":"Total Synthesis of Lyconesidine B, a <i>Lycopodium</i> Alkaloid with an Oxygenated, Amine-Type Fawcettimine Core"}]},{"@id":"https://cir.nii.ac.jp/crid/1360283689649729024","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Umpolung Reactions of α-Imino Esters: Useful Methods for the Preparation of α-Amino Acid Frameworks"}]},{"@id":"https://cir.nii.ac.jp/crid/1360283694073668224","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Formation of Isomerized <i>E</i>,<i>Z</i>-Configured 1,3-Dienes in Construction of Macrocyclic Trienes by Diene-Ene RCM"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285707430308864","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Effect of the α-substituted chiral side chain on the helical conformation of N-substituted poly(p-benzamide)"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285708226116864","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Axially Chiral Macrocyclic <i>E</i>-Alkene Bearing Bisazole Component Formed by Sequential C–H Homocoupling and Ring-Closing Metathesis"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848657454993024","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Stereoselective synthesis of tetrahydroisoquinoline alkaloids: (−)-trolline, (+)-crispin A, (+)-oleracein E"}]},{"@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":"10.1021/ol047356q"},{"@type":"CROSSREF","@value":"10.1002/anie.201500459_references_DOI_8U5f1zr6FTuRd3kTuXDl0BohFLw"},{"@type":"CROSSREF","@value":"10.1016/j.tet.2011.09.033_references_DOI_8U5f1zr6FTuRd3kTuXDl0BohFLw"},{"@type":"CROSSREF","@value":"10.1021/ol300755y_references_DOI_8U5f1zr6FTuRd3kTuXDl0BohFLw"},{"@type":"CROSSREF","@value":"10.1002/tcr.201500267_references_DOI_8U5f1zr6FTuRd3kTuXDl0BohFLw"},{"@type":"CROSSREF","@value":"10.1002/ange.201500459_references_DOI_8U5f1zr6FTuRd3kTuXDl0BohFLw"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20220049_references_DOI_8U5f1zr6FTuRd3kTuXDl0BohFLw"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20160265_references_DOI_8U5f1zr6FTuRd3kTuXDl0BohFLw"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.0c03816_references_DOI_8U5f1zr6FTuRd3kTuXDl0BohFLw"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20140250_references_DOI_8U5f1zr6FTuRd3kTuXDl0BohFLw"},{"@type":"CROSSREF","@value":"10.1016/j.polymer.2017.11.066_references_DOI_8U5f1zr6FTuRd3kTuXDl0BohFLw"}]}