{"@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/1390282679119703552.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1246/bcsj.20120105"}},{"identifier":{"@type":"COI","@value":"1:CAS:528:DC%2BC38XhsFWrsbzM"}},{"identifier":{"@type":"NDL_BIB_ID","@value":"023940272"}},{"identifier":{"@type":"URI","@value":"http://id.ndl.go.jp/bib/023940272"}},{"identifier":{"@type":"URI","@value":"https://ndlsearch.ndl.go.jp/books/R000000004-I023940272"}},{"identifier":{"@type":"URI","@value":"https://academic.oup.com/bcsj/article-pdf/85/9/1014/56274204/bcsj.20120105.pdf"}},{"identifier":{"@type":"DOI","@value":"10.1002/chin.201303026"}},{"identifier":{"@type":"NAID","@value":"130004153114"}},{"identifier":{"@type":"NAID","@value":"10031030086"}}],"resourceType":"学術雑誌論文(journal article)","dc:title":[{"@language":"en","@value":"Enantioselective Addition of Diethylzinc to Aldehydes Catalyzed by (<i>S</i>)-1-Alkyl-2-(arylamino)methylpyrrolidine"},{"@value":"Enantioselective Addition of Diethylzinc to Aldehydes Catalyzed by (S)-1-Alkyl-2-(arylamino)methylpyrrolidine"},{"@value":"ChemInform Abstract: Enantioselective Addition of Diethylzinc to Aldehydes Catalyzed by (S)‐1‐Alkyl‐2‐(arylamino)methylpyrrolidine."}],"dc:language":"en","description":[{"type":"abstract","notation":[{"@language":"en","@value":"Several chiral diamines, (<i>S</i>)-1-alkyl-2-(arylamino)methylpyrrolidine, were used as chiral catalysts for the enantioselective addition of diethylzinc to aldehydes. The best results were obtained by employing 0.15 equiv of (<i>S</i>)-2-anilinomethyl-1-benzylpyrrolidine, and chiral secondary alcohols were obtained with high enantiomeric excesses (up to 94% ee)."}],"abstractLicenseFlag":"disallow"}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1410282679119703553","@type":"Researcher","personIdentifier":[{"@type":"NRID","@value":"9000256029654"},{"@type":"NRID","@value":"9000107385222"}],"foaf:name":[{"@language":"en","@value":"Hosoda Naoya"}],"jpcoar:affiliationName":[{"@language":"en","@value":"Department of Advanced Materials Chemistry, Graduate School of Engineering, Yokohama National University"}]},{"@id":"https://cir.nii.ac.jp/crid/1410282679119703554","@type":"Researcher","personIdentifier":[{"@type":"NRID","@value":"9000256029655"},{"@type":"NRID","@value":"9000107385223"}],"foaf:name":[{"@language":"en","@value":"Ito Hiroki"}],"jpcoar:affiliationName":[{"@language":"en","@value":"Department of Advanced Materials Chemistry, Graduate School of Engineering, Yokohama National University"}]},{"@id":"https://cir.nii.ac.jp/crid/1410282679119703552","@type":"Researcher","personIdentifier":[{"@type":"NRID","@value":"9000256029656"},{"@type":"NRID","@value":"9000107385224"}],"foaf:name":[{"@language":"en","@value":"Takimoto Tatsuya"}],"jpcoar:affiliationName":[{"@language":"en","@value":"Department of Advanced Materials Chemistry, Graduate School of Engineering, Yokohama National University"}]},{"@id":"https://cir.nii.ac.jp/crid/1030003658312732290","@type":"Researcher","personIdentifier":[{"@type":"KAKEN_RESEARCHERS","@value":"20134439"},{"@type":"NRID","@value":"1000020134439"},{"@type":"NRID","@value":"9000283395575"},{"@type":"NRID","@value":"9000007276532"},{"@type":"NRID","@value":"9000000125004"},{"@type":"NRID","@value":"9000256029657"},{"@type":"NRID","@value":"9000021821167"},{"@type":"NRID","@value":"9000313199798"},{"@type":"NRID","@value":"9000283372608"},{"@type":"NRID","@value":"9000258597746"},{"@type":"NRID","@value":"9000257715704"},{"@type":"NRID","@value":"9000020295955"},{"@type":"NRID","@value":"9000021820785"},{"@type":"NRID","@value":"9000255702458"},{"@type":"NRID","@value":"9000258594149"},{"@type":"NRID","@value":"9000016386561"},{"@type":"NRID","@value":"9000298897146"},{"@type":"NRID","@value":"9000002105397"},{"@type":"NRID","@value":"9000107385225"},{"@type":"NRID","@value":"9000257731215"},{"@type":"NRID","@value":"9000257726364"},{"@type":"NRID","@value":"9000010567026"},{"@type":"NRID","@value":"9000000618267"},{"@type":"NRID","@value":"9000001222202"},{"@type":"NRID","@value":"9000253128447"},{"@type":"NRID","@value":"9000001881860"},{"@type":"NRID","@value":"9000283741420"},{"@type":"NRID","@value":"9000347163316"},{"@type":"NRID","@value":"9000253130118"},{"@type":"NRID","@value":"9000258595558"},{"@type":"NRID","@value":"9000257720139"},{"@type":"RESEARCHMAP","@value":"https://researchmap.jp/read0009119"}],"foaf:name":[{"@language":"en","@value":"Asami Masatoshi"}],"jpcoar:affiliationName":[{"@language":"en","@value":"Department of Advanced Materials Chemistry, Graduate School of Engineering, Yokohama National University"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"00092673"},{"@type":"LISSN","@value":"00092673"},{"@type":"EISSN","@value":"13480634"},{"@type":"NDL_BIB_ID","@value":"000000118949"},{"@type":"ISSN","@value":"00092673"},{"@type":"PISSN","@value":"09317597"},{"@type":"EISSN","@value":"15222667"},{"@type":"NCID","@value":"AA00580132"}],"prism:publicationName":[{"@language":"en","@value":"Bulletin of the Chemical Society of Japan"},{"@language":"en","@value":"Bull. Chem. Soc. Jpn."}],"dc:publisher":[{"@language":"en","@value":"The Chemical Society of Japan"},{"@language":"ja","@value":"公益社団法人 日本化学会"}],"prism:publicationDate":"2012","prism:volume":"85","prism:number":"9","prism:startingPage":"1014","prism:endingPage":"1022"},"reviewed":"false","url":[{"@id":"http://id.ndl.go.jp/bib/023940272"},{"@id":"https://ndlsearch.ndl.go.jp/books/R000000004-I023940272"},{"@id":"https://academic.oup.com/bcsj/article-pdf/85/9/1014/56274204/bcsj.20120105.pdf"}],"availableAt":"2012","project":[{"@id":"https://cir.nii.ac.jp/crid/1040000782208589184","@type":"Project","projectIdentifier":[{"@type":"KAKEN","@value":"24550113"},{"@type":"JGN","@value":"JP24550113"},{"@type":"URI","@value":"https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-24550113/"}],"notation":[{"@language":"ja","@value":"キラルな二置換オルトキシリレン誘導体を活用する高選択的不斉触媒反応の開発"},{"@language":"en","@value":"Catalytic asymmetric reactions by the use of chiral o-xylylene derivatives"}]},{"@id":"https://cir.nii.ac.jp/crid/1040282257197419648","@type":"Project","projectIdentifier":[{"@type":"KAKEN","@value":"24655203"},{"@type":"JGN","@value":"JP24655203"},{"@type":"URI","@value":"https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-24655203/"}],"notation":[{"@language":"ja","@value":"キラル配位子を有する高分子ゲルの合成と不斉合成触媒への展開"}]}],"relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1360002219107321984","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"EFFICIENT ASYMMETRIC INDUCTION VIA COORDINATION OF CHIRAL DIAMINE TO TIN(II) ENOLATE: A HIGHLY ENANTIOSELECTIVE SYNTHESIS OF 2-SUBSTITUTED MALATES"}]},{"@id":"https://cir.nii.ac.jp/crid/1360002219109907328","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Catalytic Asymmetric Borane Reduction of Prochiral Ketones by the Use of Chiral <i>β</i>-Diamines"}]},{"@id":"https://cir.nii.ac.jp/crid/1360002219109927424","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"An Efficient Enantioselective Preparation of (<i>S,S</i>)-1,2-Bis(1-hydroxyalkyl)benzene"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011144129142656","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Chiral ligands containing heteroatoms. 8. 2-[(2s)-2-pyrrolidinyl]pyridine as a novel catalyst in the enantioselective addition of diethylzinc to aldehydes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011144567228416","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Catalytic Asymmetric Organozinc Additions to Carbonyl Compounds"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011144728811520","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"New highly efficient aziridine-functionalized tridentate sulfinyl catalysts for enantioselective diethylzinc addition to carbonyl compounds"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011146543006208","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Kinetic Resolution of cis-3-Alkylcyclohexene Oxide by a Chiral Lithium Amide - An Application to a Synthesis of Both Enantiomers of Isomenthon -"}]},{"@id":"https://cir.nii.ac.jp/crid/1360283694078545280","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The Enantioselective Michael Addition of Thiols to Cycloalkenones by Using (2<i>S</i>, 4<i>S</i>)-2-Anilinomethyl-1-ethyl-4-hydroxypyrrolidine as Chiral Catalyst"}]},{"@id":"https://cir.nii.ac.jp/crid/1360283694081972736","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Catalytic Asymmetric Borane Reduction of Prochiral Ketones by Using (<i>S</i>)-2-(Anilinomethyl)pyrrolidine"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285707501714048","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of chiral 2-(anilinophenylmethyl)pyrrolidines and 2-(anilinodiphenylmethyl)pyrrolidine and their application to enantioselective borane reduction of prochiral ketones as chiral catalysts"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292619004730752","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Catalytic asymmetric borane reduction of prochiral ketones by the use of diazaborolidine catalysts prepared from chiral β-diamines"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292620598127104","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"(1R,5R)-1-(1′-Dimethylaminoethyl)-2-isopropylidene-5-methylcyclohexanol as a Chiral Ligand in the Enantioselective Addition of Diethylzinc to Aldehydes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574095356221056","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of Novel Derivatives of (1<i>S</i>,4<i>S</i>)‐2,5‐Diazabicyclo[2.2.1]heptane and Their Evaluation as Potential Ligands in Asymmetric Catalysis"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574095875281664","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of chiral ligands containing the N-(S)-α-phenylethyl group and their evaluation as activators in the enantioselective addition of Et2Zn to benzaldehyde"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574096565119616","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Structurally constrained C1-1,1′-bisisoquinoline-based chiral ligands: geometrical implications on enantioinduction in the addition of diethylzinc to aldehydes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360846644031050112","@type":"Article","relationType":["references","cites"],"jpcoar:relatedTitle":[{"@value":"Asymmetric Reduction of Prochiral Ketones with Chiral Hydride Reagents Prepared from Lithium Aluminium Hydride and (<i>S</i>)-2-(<i>N</i>-Substituted aminomethyl)pyrrolidines"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855569212985472","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Enantioselective addition of diethylzinc to aldehydes catalyzed by a β-amino alcohol derived from (+)-3-carene"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855569257171712","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Enantioselective diethylzinc addition to aromatic and aliphatic aldehydes using (3R,5R)-dihydroxypiperidine derivatives catalyst"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137043460885376","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Chiral ligands derived from abrine. Part 6: Importance of a bulky N-alkyl group in indole-containing chiral β-tertiary amino alcohols for controlling enantioselectivity in addition of diethylzinc toward aldehydes"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137045328071552","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Asymmetric aldol reaction between achiral silyl enol ethers and achiral aldehydes by use of a chiral promoter system"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137046513984512","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A New Cysteine-Derived Ligand as Catalyst for the Addition of Diethylzinc to Aldehydes: The Importance of a ‘Free’ Sulfide Site for Enantioselectivity"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418519188943360","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Catalytic enantioselective rearrangement of meso-epoxides mediated by chiral lithium amides in the presence of excess cross-linked polymer-bound lithium amides"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418519597398784","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Enantioselective addition of diethylzinc to benzaldehyde catalyzed by a small amount of chiral 2-amino-1-alcohols"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418520656231552","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Syntheses of new chiral 1,2-diamines and δ-amino-alcohols and their application in catalytic enantioselective CC bond formations at an elevated temperature of up to 110 °C"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418520936513280","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Catalytic asymmetric induction. Highly enantioselective addition of dialkylzincs to aldehydes using chiral pyrrolidinylmethanols and their metal salts"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699993593021824","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A chiral disulfide derived from (R)-cysteine in the enantioselective addition of diethylzinc to aldehydes: loading effect and asymmetric amplification"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699993782642048","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Enantioselective addition of dialkylzinc to aldehydes catalyzed by (S)-2-(N,N-disubstituted aminomethyl)indoline"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699994897416576","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The application of chiral amino thiols as catalysts in the enantioselective addition of diethylzinc to aldehydes"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981470845412608","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Modular Ligands Derived from Amino Acids for the Enantioselective Addition of Organozinc Reagents to Aldehydes"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981471090492160","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"New chiral tetraaza ligands for the efficient enantioselective addition of dialkylzinc to aromatic aldehydes"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262944060199680","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Catalytic asymmetric induction.  Highly enantioselective addition of dialkylzincs to aldehydes"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262944321740160","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Switching of Enantioselectivity in the Catalytic Addition of Diethylzinc to Aldehydes by Regioisomeric Chiral 1,3-Amino Sulfonamide Ligands"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262946256312448","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of new chiral cis-3-aminoazetidines and their use in catalytic asymmetric reactions"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825895846327296","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Chiral amide from (1S,2R)-(+)-norephedrine alkaloid in the enantioselective addition of diethylzinc to aryl and heteroaryl aldehydes"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107368784902656","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of chiral ligands derived from the Betti base and their use in the enantioselective addition of diethylzinc to aromatic aldehydes"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107369288421376","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Perhydro-1,3-benzoxazines derived from (−)-8-aminomenthol as ligands for the catalytic enantioselective addition of diethylzinc to aldehydes"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107369408278272","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Enantioselective addition of organozinc reagents to aldehydes"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107370125643648","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A convenient synthesis of piperidine-based β-amino alcohols from l-Phe and highly enantioselective addition of diethyl zinc to aldehydes"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107370908215552","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Chiral Sulfur Ligands for Asymmetric Catalysis"}]},{"@id":"https://cir.nii.ac.jp/crid/1363670320083745152","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of a series of novel N,N-dialkyl-TsDPEN ligands and their application to enantioselective addition of dialkylzinc to benzaldehyde"}]},{"@id":"https://cir.nii.ac.jp/crid/1363670320889461120","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis and application of chiral β‐amino disulfides as ligands for the enantioselective addition of diethylzinc to aldehydes"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951795686251136","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Structural Optimization of Enantiopure 2-Cyclialkylamino-2-aryl-1,1-diphenylethanols as Catalytic Ligands for Enantioselective Additions to Aldehydes"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951795743214208","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Enantioselective ethylation of aldehydes with 1,3-N-donor ligands derived from (+)-camphoric acid"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951796275613824","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Asymmetric addition of diethylzinc to aldehydes catalyzed by a camphor-derived β-amino alcohol"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233270465521152","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of new chiral imidazolidine disulfides derived from l-cystine and their application in the enantioselective addition of diethylzinc to aldehydes"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233270734558464","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Enantioselective Addition of Organometallic Reagents to Carbonyl Compounds: Chirality Transfer, Multiplication, and Amplification"}]},{"@id":"https://cir.nii.ac.jp/crid/1390001206216703360","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@language":"ja","@value":"1-Azabicyclo化合物の研究(第21報)1,2,3,10,11,11a-Hexahydro-5H-pyrrolo-[2,1-c][1,4]benzodiazepin-11-oneおよび5,6,6a, 7,8,9,10,12-Octahydropyrido[2,1-c][1,4]benzodiazepin-6-oneから中環状AminolactamおよびSpiroaminolactam体の合成"},{"@language":"en","@value":"Studies on 1-Azabicyclo Compounds. XXI. Synthesis of Medium Ring Aminolactams and Spiroaminolactams from 1, 2, 3, 10, 11, 11a-Hexahydro-5H-pyrrolo[2, 1-c][1, 4]benzodiazepin-11-one and 5, 6, - 6a, 7, 8, 9, 10, 12-Octahydropyrido[2, 1-c][1, 4]- benzodiazepin-6-one"}]},{"@id":"https://cir.nii.ac.jp/crid/1522262179614828160","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Enantioselective Addition of Diethylzinc to Aldehydes Catalyzed by (S)-2-(N,N-Disubstituted aminomethyl)pyrrolidine"},{"@language":"ja-Kana","@value":"Enantioselective Addition of Diethylzin"}]},{"@id":"https://cir.nii.ac.jp/crid/1522825130027119744","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Chiral Porous TADDOL-Embedded Organic Polymers for Asymmetric Diethylzinc Addition to Aldehydes"}]},{"@id":"https://cir.nii.ac.jp/crid/1570009751233270912","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1570009751233844736","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1570009751233848448","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1570291226209972608","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1570291226209975552","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1570291226209979136","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1570291226780332928","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1570572701187264128","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1570572701187266176","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1570572701187268608","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1570572701187270272","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1570854176163972864","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1570854176163976320","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1570854176163979776","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1571135651140112128","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1571135651140113664","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1571135651140685056","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1571135651140686336","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1571135651140688512","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1571135651140692096","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1571135651469033088","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1571417126116817664","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1571417126117396736","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1571417126117397760","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1571980076070245504","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1571980076070817408","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1571980076070819584","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1571980076070820736","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1571980076070823296","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1572261551046950528","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1572261551047525632","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1572261551047526784","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1572261551047530240","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1572543026023666816","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1572824501000374016","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1572824501000377472","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1572824501000949376","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1572824501000953984","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1572824501000955648","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1573105975977658368","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1573105975977662464","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1573105975977663488","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1573105975977665664","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1573105975977666560","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1573668925931084672","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1573668925931087232","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1573950399810471680","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1574231875883927040","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1574231875884505088","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1574231875884507392","@type":"Article","relationType":["cites"]},{"@id":"https://cir.nii.ac.jp/crid/1574231875884508416","@type":"Article","relationType":["cites"]}],"dataSourceIdentifier":[{"@type":"JALC","@value":"oai:japanlinkcenter.org:1000889444"},{"@type":"NDL_SEARCH","@value":"oai:ndlsearch.ndl.go.jp:R000000004-I023940272"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20120105"},{"@type":"CIA","@value":"130004153114"},{"@type":"CIA","@value":"10031030086"},{"@type":"KAKEN","@value":"PRODUCT-14650398"},{"@type":"KAKEN","@value":"PRODUCT-14763444"},{"@type":"OPENAIRE","@value":"doi_dedup___::f79f7fdea50186a09289ba49dc032a79"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20130317_references_DOI_D6iodwrdVbvc0bHGV6PeS48UdHf"},{"@type":"CROSSREF","@value":"10.1016/j.tet.2012.12.024_references_DOI_D6iodwrdVbvc0bHGV6PeS48UdHf"}]}