{"@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/1361699994477112704.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1039/c4cc03826f"}},{"identifier":{"@type":"URI","@value":"http://pubs.rsc.org/en/content/articlepdf/2014/CC/C4CC03826F"}}],"dc:title":[{"@value":"Tertiary amide-based Knoevenagel-type reactions: a direct, general, and chemoselective approach to enaminones"}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1381699994477112704","@type":"Researcher","foaf:name":[{"@value":"Pei-Qiang Huang"}]},{"@id":"https://cir.nii.ac.jp/crid/1381699994477112707","@type":"Researcher","foaf:name":[{"@value":"Wei Ou"}]},{"@id":"https://cir.nii.ac.jp/crid/1381699994477112706","@type":"Researcher","foaf:name":[{"@value":"Kai-Jiong Xiao"}]},{"@id":"https://cir.nii.ac.jp/crid/1381699994477112705","@type":"Researcher","foaf:name":[{"@value":"Ai-E Wang"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"13597345"},{"@type":"EISSN","@value":"1364548X"}],"prism:publicationName":[{"@value":"Chemical Communications"}],"dc:publisher":[{"@value":"Royal Society of Chemistry (RSC)"}],"prism:publicationDate":"2014-06-26","prism:volume":"50","prism:number":"63","prism:startingPage":"8761"},"reviewed":"false","url":[{"@id":"http://pubs.rsc.org/en/content/articlepdf/2014/CC/C4CC03826F"}],"createdAt":"2014-06-19","modifiedAt":"2024-04-17","relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1360004229991516416","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Chemoselective Reductive Nucleophilic Addition to Tertiary Amides, Secondary Amides, and <i>N</i>‐Methoxyamides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360283691637094784","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Unified Total Synthesis of Stemoamide-Type Alkaloids by Chemoselective Assembly of Five-Membered Building Blocks"}]},{"@id":"https://cir.nii.ac.jp/crid/1360565166566126336","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Iridium-Catalyzed Chemoselective Reductive Nucleophilic Addition to <i>N</i>-Methoxyamides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360565166613507840","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"An Iridium-Catalyzed Reductive Approach to Nitrones from <i>N</i>-Hydroxyamides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848658559665408","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total synthesis of complex alkaloids by nucleophilic addition to amides"}]},{"@id":"https://cir.nii.ac.jp/crid/1390001204141606272","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Reductive Approach to Nitrones from <i>N</i>-Siloxyamides and <i>N</i>-Hydroxyamides"},{"@value":"BCSJ Award Article : Reductive Approach to Nitrones from N-Siloxyamides and N-Hydroxyamides"},{"@value":"Reductive approach to nitrones from N-siloxyamides and N-hydroxyamides"}]},{"@id":"https://cir.nii.ac.jp/crid/1390001204143489664","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Total Syntheses of (±)-Gephyrotoxin and (±)-Perhydrogephyrotoxin"},{"@value":"BCSJ Award Article : Total Syntheses of (±)-Gephyrotoxin and (±)-Perhydrogephyrotoxin"},{"@value":"ChemInform Abstract: Total Syntheses of (.+‐.)‐Gephyrotoxin and (.+‐.)‐Perhydrogephyrotoxin."}]},{"@id":"https://cir.nii.ac.jp/crid/1390282680316901376","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"ja","@value":"<i>N</i>-アルコキシアミド基への求核付加反応の開発とゲフィロトキシンの全合成"},{"@language":"en","@value":"Nucleophilic Addition to <i>N</i>-Alkoxyamides: Development and Application to the Total Synthesis of Gephyrotoxin"},{"@value":"N-アルコキシアミド基への求核付加反応の開発とゲフィロトキシンの全合成"},{"@language":"ja-Kana","@value":"N-アルコキシアミドキ エ ノ キュウカク フカ ハンノウ ノ カイハツ ト ゲフィロトキシン ノ ゼン ゴウセイ"}]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1039/c4cc03826f"},{"@type":"CROSSREF","@value":"10.1002/chem.201404648_references_DOI_AI3YqCU9MlYE7OOcMFHlJyGYUcS"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20140398_references_DOI_AI3YqCU9MlYE7OOcMFHlJyGYUcS"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20170086_references_DOI_AI3YqCU9MlYE7OOcMFHlJyGYUcS"},{"@type":"CROSSREF","@value":"10.1039/c8ob00733k_references_DOI_AI3YqCU9MlYE7OOcMFHlJyGYUcS"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.74.599_references_DOI_AI3YqCU9MlYE7OOcMFHlJyGYUcS"},{"@type":"CROSSREF","@value":"10.1021/jacs.6b02324_references_DOI_AI3YqCU9MlYE7OOcMFHlJyGYUcS"},{"@type":"CROSSREF","@value":"10.1021/jacs.7b10944_references_DOI_AI3YqCU9MlYE7OOcMFHlJyGYUcS"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.5b00664_references_DOI_AI3YqCU9MlYE7OOcMFHlJyGYUcS"}]}