{"@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/1360002216612923264.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1021/acs.orglett.7b01213"}},{"identifier":{"@type":"URI","@value":"https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b01213"}},{"identifier":{"@type":"PMID","@value":"28558220"}}],"resourceType":"学術雑誌論文(journal article)","dc:title":[{"@value":"Carboxylate Anions Accelerate Pyrrolidinopyridine (PPy)-Catalyzed Acylation: Catalytic Site-Selective Acylation of a Carbohydrate by in Situ Counteranion Exchange"}],"description":[{"notation":[{"@value":"Acylpyridinium ions have been known as catalytically active species in acylation reactions catalyzed by 4-dimethylaminopyridine and its analogues. Acylpyridinium carboxylates were found to be 800-1300 times more reactive than the corresponding acylpyridinium chlorides. A catalytic cycle was developed, in which acylpyridinium carboxylates were generated by in situ counteranion exchange from the acylpyridinium chlorides. A catalyst loading as low as 0.01 mol % and catalyst turnover number of up to 6700 were achieved for site-selective acylation of a carbohydrate."}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1380566394752234112","@type":"Researcher","foaf:name":[{"@value":"Masanori Yanagi"}],"jpcoar:affiliationName":[{"@value":"Institute for Chemical Research, Kyoto University, Uji 611-0011, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1380566394752234115","@type":"Researcher","foaf:name":[{"@value":"Ayumi Imayoshi"}],"jpcoar:affiliationName":[{"@value":"Institute for Chemical Research, Kyoto University, Uji 611-0011, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1380566394752234114","@type":"Researcher","foaf:name":[{"@value":"Yoshihiro Ueda"}],"jpcoar:affiliationName":[{"@value":"Institute for Chemical Research, Kyoto University, Uji 611-0011, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1380566394752234113","@type":"Researcher","foaf:name":[{"@value":"Takumi Furuta"}],"jpcoar:affiliationName":[{"@value":"Institute for Chemical Research, Kyoto University, Uji 611-0011, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1420845751162553984","@type":"Researcher","personIdentifier":[{"@type":"KAKEN_RESEARCHERS","@value":"50214680"},{"@type":"NRID","@value":"1000050214680"},{"@type":"ORCID","@value":"0000-0002-9959-0420"},{"@type":"NRID","@value":"9000006703763"},{"@type":"NRID","@value":"9000006764451"},{"@type":"NRID","@value":"9000020321450"},{"@type":"NRID","@value":"9000391962548"},{"@type":"NRID","@value":"9000283740506"},{"@type":"NRID","@value":"9000252801109"},{"@type":"NRID","@value":"9000264273175"},{"@type":"NRID","@value":"9000000791715"},{"@type":"NRID","@value":"9000010549055"},{"@type":"NRID","@value":"9000002145021"},{"@type":"NRID","@value":"9000006774974"},{"@type":"NRID","@value":"9000326650781"},{"@type":"NRID","@value":"9000326650761"},{"@type":"NRID","@value":"9000254697767"},{"@type":"NRID","@value":"9000006764593"},{"@type":"NRID","@value":"9000005182343"},{"@type":"NRID","@value":"9000024532885"},{"@type":"NRID","@value":"9000023188186"},{"@type":"NRID","@value":"9000312259573"},{"@type":"NRID","@value":"9000326650742"},{"@type":"NRID","@value":"9000002002378"},{"@type":"NRID","@value":"9000018233246"},{"@type":"NRID","@value":"9000024512842"},{"@type":"NRID","@value":"9000024565768"},{"@type":"NRID","@value":"9000254713350"},{"@type":"NRID","@value":"9000399239121"},{"@type":"NRID","@value":"9000237869315"},{"@type":"NRID","@value":"9000332225352"},{"@type":"NRID","@value":"9000326650775"},{"@type":"NRID","@value":"9000406228345"},{"@type":"NRID","@value":"9000402379936"},{"@type":"NRID","@value":"9000250182836"},{"@type":"NRID","@value":"9000400161982"},{"@type":"NRID","@value":"9000257732519"},{"@type":"NRID","@value":"9000024533303"},{"@type":"NRID","@value":"9000254689675"},{"@type":"NRID","@value":"9000254715376"},{"@type":"NRID","@value":"9000252669748"},{"@type":"NRID","@value":"9000024447955"},{"@type":"NRID","@value":"9000023685667"},{"@type":"NRID","@value":"9000242447906"},{"@type":"NRID","@value":"9000254689849"},{"@type":"NRID","@value":"9000411003298"},{"@type":"NRID","@value":"9000016386429"},{"@type":"NRID","@value":"9000006764604"},{"@type":"NRID","@value":"9000024549685"},{"@type":"NRID","@value":"9000023340305"},{"@type":"NRID","@value":"9000391964857"},{"@type":"NRID","@value":"9000257731210"},{"@type":"NRID","@value":"9000345216202"},{"@type":"NRID","@value":"9000006764623"},{"@type":"NRID","@value":"9000311776820"},{"@type":"NRID","@value":"9000253120664"},{"@type":"NRID","@value":"9000254709222"},{"@type":"NRID","@value":"9000010624563"},{"@type":"NRID","@value":"9000023677116"},{"@type":"NRID","@value":"9000392869610"},{"@type":"NRID","@value":"9000005166267"},{"@type":"NRID","@value":"9000254218225"},{"@type":"NRID","@value":"9000242448234"},{"@type":"RESEARCHMAP","@value":"https://researchmap.jp/TakeoKawabata"}],"foaf:name":[{"@value":"Takeo Kawabata"}],"jpcoar:affiliationName":[{"@value":"Institute for Chemical Research, Kyoto University, Uji 611-0011, Japan"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"15237060"},{"@type":"EISSN","@value":"15237052"}],"prism:publicationName":[{"@value":"Organic Letters"}],"dc:publisher":[{"@value":"American Chemical Society (ACS)"}],"prism:publicationDate":"2017-05-30","prism:volume":"19","prism:number":"12","prism:startingPage":"3099","prism:endingPage":"3102"},"reviewed":"false","url":[{"@id":"https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.7b01213"}],"createdAt":"2017-05-30","modifiedAt":"2023-04-26","project":[{"@id":"https://cir.nii.ac.jp/crid/1040000781894479360","@type":"Project","projectIdentifier":[{"@type":"KAKEN","@value":"16H01148"},{"@type":"JGN","@value":"JP16H01148"},{"@type":"URI","@value":"https://kaken.nii.ac.jp/grant/KAKENHI-PUBLICLY-16H01148/"}],"notation":[{"@language":"ja","@value":"糖関連中分子の位置選択的精密合成"}]},{"@id":"https://cir.nii.ac.jp/crid/1040282257257430144","@type":"Project","projectIdentifier":[{"@type":"KAKEN","@value":"26221301"},{"@type":"JGN","@value":"JP26221301"},{"@type":"URI","@value":"https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-26221301/"}],"notation":[{"@language":"ja","@value":"多官能基性化合物の位置選択的分子変換"},{"@language":"en","@value":"Regioselective Molecular Transforamtion of Mutifunctionalized Molecules"}]}],"relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1050001335688299392","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Perfectly regioselective acylation of a cardiac glycoside, digitoxin, via catalytic amplification of the intrinsic reactivity"}]},{"@id":"https://cir.nii.ac.jp/crid/1050001335818800256","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Total Synthesis of Ellagitannins through Regioselective Sequential Functionalization of Unprotected Glucose."}]},{"@id":"https://cir.nii.ac.jp/crid/1050574036206257920","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Enantioselective preparation of mechanically planar chiral rotaxanes by kinetic resolution strategy"}]},{"@id":"https://cir.nii.ac.jp/crid/1050845760748957824","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Final-Stage Site-Selective Acylation for the Total Syntheses of Multifidosides A-C."},{"@value":"Final‐Stage Site‐Selective Acylation for the Total Syntheses of Multifidosides A–C"}]},{"@id":"https://cir.nii.ac.jp/crid/1360002219106117888","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Total Synthesis of Cercidinin A via a Sequential Site-selective Acylation Strategy"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004229919437184","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Investigation of the Carboxylate Position during the Acylation Reaction Catalyzed by Biaryl DMAP Derivatives with an Internal Carboxylate"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004232528076544","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Recent topics in enantioselective acyl transfer reactions with dialkylaminopyridine-based nucleophilic catalysts"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011145220208896","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Site-Selective Reactions with Peptide-Based Catalysts"}]},{"@id":"https://cir.nii.ac.jp/crid/1360017279842559232","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Approach Toward Reversal of Chemoselectivity in Catalytic Silylation of Pyranosides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360283689685911424","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Organocatalytic Site-Selective Acylation of Carbohydrates and Polyol Compounds"}]},{"@id":"https://cir.nii.ac.jp/crid/1360283691645520896","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Regioselective Diversification of a Cardiac Glycoside, Lanatoside C, by Organocatalysis"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285704859538176","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Insights into the Molecular Recognition Process in Organocatalytic Chemoselective Monoacylation of 1,5‐Pentanediol"}]},{"@id":"https://cir.nii.ac.jp/crid/1360294643823417088","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Acylative kinetic resolution of 1,1′-binaphthyl-8,8′-diamines by organocatalysis"}]},{"@id":"https://cir.nii.ac.jp/crid/1360565166622627456","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Functional Group Tolerance in Organocatalytic Regioselective Acylation of Carbohydrates"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567179870482432","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Organocatalytic Chemoselective Monoacylation of 1,<i>n</i>‐Linear Diols"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567183183526784","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Origin of High<i>E</i>-Selectivity in 4-Pyrrolidinopyridine-Catalyzed Tetrasubstituted α,α′-Alkenediol: A Computational and Experimental Study"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574094966910080","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Chiral Dialkylaminopyridine Catalysts in Asymmetric Synthesis"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574094969698304","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Desymmetrisation of meso-diols mediated by non-enzymatic acyl transfer catalysts"}]},{"@id":"https://cir.nii.ac.jp/crid/1360588380607544064","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Sequential Site-Selective Functionalization: A Strategy for Total Synthesis of Natural Glycosides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360849942940661120","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of 4-Deoxy Pyranosides via Catalyst-Controlled Site-Selective Toluoylation of Abundant Sugars"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855568895928064","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Site-Selective Catalysis"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855569720764288","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Counterion-Directed Regioselective Acetylation of Octyl β-<scp>d</scp>-Glucopyranoside"}]},{"@id":"https://cir.nii.ac.jp/crid/1360869854343130624","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Unified Strategy for the Concise Total Syntheses of All Six 3″-<i>O</i>-Acyl Quercitrins Based on Regioselective Acylation Catalyzed by Boronic Acid"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137043452311936","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Plant Polyphenols: Chemical Properties, Biological Activities, and Synthesis"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137043972976512","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A Catalytic One-Step Process for the Chemo- and Regioselective Acylation of Monosaccharides"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137044264097664","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Nucleophilic Catalysis by 4‐(Dialkylamino)pyridines Revisited—The Search for Optimal Reactivity and Selectivity"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137045826563968","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Pursuit of Noncovalent Interactions for Strategic Site-Selective Catalysis"}]},{"@id":"https://cir.nii.ac.jp/crid/1361412889448682496","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Chiral Benzazaborole‐Catalyzed Regioselective Sulfonylation of Unprotected Carbohydrate Derivatives"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418521043085696","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Harnessing non-covalent interactions to exert control over regioselectivity and site-selectivity in catalytic reactions"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699993920235264","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The DMAP‐Catalyzed Acetylation of Alcohols—A Mechanistic Study (DMAP=4‐(Dimethylamino)pyridine)"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699996193722240","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Organocatalytic Enantioselective Acyl Transfer onto Racemic as well as <i>meso</i> Alcohols, Amines, and Thiols"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699996268176384","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Theoretical Prediction of Selectivity in Kinetic Resolution of Secondary Alcohols Catalyzed by Chiral DMAP Derivatives"}]},{"@id":"https://cir.nii.ac.jp/crid/1361975842847474560","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Catalytic Activation of <i>Cis</i>-Vicinal Diols by Boronic Acids: Site-Selective Acylation of Carbohydrates"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981469128538880","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Kinetic resolution strategies using non-enzymatic catalysts"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981470545788160","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Nucleophilic Chiral Amines as Catalysts in Asymmetric Synthesis"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981470776526976","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Ellagitannin Chemistry"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262943713527680","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Catalytic Non‐Enzymatic Kinetic Resolution"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262945376992000","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Enantioselective silyl protection of alcohols promoted by a combination of chiral and achiral Lewis basic catalysts"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544420302222208","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Phenylethanoid glycosides in plants: structure and biological activity"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107369641488384","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"4‐Dialkylaminopyridines as Highly Active Acylation Catalysts. [New synthetic method (25)]"}]},{"@id":"https://cir.nii.ac.jp/crid/1363670318638104704","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Organocatalysis: acylation catalysts"}]},{"@id":"https://cir.nii.ac.jp/crid/1363670319015457920","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Asymmetric Catalysis with “Planar-Chiral” Derivatives of 4-(Dimethylamino)pyridine"}]},{"@id":"https://cir.nii.ac.jp/crid/1363670319259327488","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Catalyst-Controlled, Regioselective Reactions of Carbohydrate Derivatives"}]},{"@id":"https://cir.nii.ac.jp/crid/1363670320524182784","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Efficiency in Nonenzymatic Kinetic Resolution"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951795002754816","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Low-loading asymmetric organocatalysis"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951795254278784","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Chemo- and site-selective derivatizations of natural products enabling biological studies"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951795696422144","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Structural Analyses of <i>N</i>‐Acetylated 4‐(Dimethylamino)pyridine (DMAP) Salts"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233270342623232","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Site-Selectivity Control in Organic Reactions: A Quest To Differentiate Reactivity among the Same Kind of Functional Groups"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233270960013824","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Kinetic Resolution of Racemic α-Arylalkanoic Acids with Achiral Alcohols via the Asymmetric Esterification Using Carboxylic Anhydrides and Acyl-Transfer Catalysts"}]},{"@id":"https://cir.nii.ac.jp/crid/1390282763102428288","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"ja","@value":"アシル化を通して見えるもの"},{"@language":"en","@value":"Potential in Acylation"},{"@value":"感動の瞬間 アシル化を通して見えるもの"},{"@language":"ja-Kana","@value":"カンドウ ノ シュンカン アシルカ オ トオシテ ミエル モノ"}]},{"@id":"https://cir.nii.ac.jp/crid/1390850247500196480","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Boronic Acid-Catalyzed Final-Stage Site-Selective Acylation for the Total Syntheses of <i>O</i>-3′-Acyl Bisabolol β-D-Fucopyranoside Natural Products and Their Analogues"},{"@value":"Boronic Acid-Catalyzed Final-Stage Site-Selective Acylation for the Total Syntheses of O-3'-Acyl Bisabolol β-D-Fucopyranoside Natural Products and Their Analogues"}]},{"@id":"https://cir.nii.ac.jp/crid/1390852514697387008","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Site-Selective Molecular Transformation: Acylation of Hydroxy Groups and C–H Amination"}]},{"@id":"https://cir.nii.ac.jp/crid/1391130851441694976","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Catalyst-Controlled Site-Selective Acylation and its Application to Unconventional Total Synthesis of Natural Glycosides"},{"@language":"ja","@value":"触媒制御型位置選択的アシル化法の開発と新規逆合成解析に基づく配糖体天然物の全合成への展開"},{"@language":"ja-Kana","@value":"ショクバイ セイギョガタ イチ センタクテキ アシルカホウ ノ カイハツ ト シンキ ギャクゴウセイ カイセキ ニ モトズク ハイトウタイ テンネンブツ ノ ゼン ゴウセイ エ ノ テンカイ"}]},{"@id":"https://cir.nii.ac.jp/crid/1523388080834270336","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"RECENT DEVELOPMENT OF STEREOSELECTIVE GLYCOSYLATION REACTIONS"}]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1021/acs.orglett.7b01213"},{"@type":"KAKEN","@value":"PRODUCT-21619398"},{"@type":"KAKEN","@value":"PRODUCT-21660451"},{"@type":"OPENAIRE","@value":"doi_dedup___::1594f91cdbc200d44dda99d6e7de4c88"},{"@type":"CROSSREF","@value":"10.1038/s41467-020-20372-0_references_DOI_VEuIWNyNiZ90YvRtY5pr47UmKBm"},{"@type":"CROSSREF","@value":"10.1002/ejoc.202200949_references_DOI_VEuIWNyNiZ90YvRtY5pr47UmKBm"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.9b01549_references_DOI_VEuIWNyNiZ90YvRtY5pr47UmKBm"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.77.268_references_DOI_VEuIWNyNiZ90YvRtY5pr47UmKBm"},{"@type":"CROSSREF","@value":"10.1016/j.tet.2021.132539_references_DOI_VEuIWNyNiZ90YvRtY5pr47UmKBm"},{"@type":"CROSSREF","@value":"10.1016/j.tetlet.2018.03.016_references_DOI_VEuIWNyNiZ90YvRtY5pr47UmKBm"},{"@type":"CROSSREF","@value":"10.1246/cl.190872_references_DOI_VEuIWNyNiZ90YvRtY5pr47UmKBm"},{"@type":"CROSSREF","@value":"10.1248/cpb.c21-00425_references_DOI_VEuIWNyNiZ90YvRtY5pr47UmKBm"},{"@type":"CROSSREF","@value":"10.3987/rev-20-933_references_DOI_VEuIWNyNiZ90YvRtY5pr47UmKBm"},{"@type":"CROSSREF","@value":"10.1007/978-981-97-1619-7_20_references_DOI_VEuIWNyNiZ90YvRtY5pr47UmKBm"},{"@type":"CROSSREF","@value":"10.1248/cpb.c20-00834_references_DOI_VEuIWNyNiZ90YvRtY5pr47UmKBm"},{"@type":"CROSSREF","@value":"10.1021/acs.joc.4c02659_references_DOI_VEuIWNyNiZ90YvRtY5pr47UmKBm"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.9b01231_references_DOI_VEuIWNyNiZ90YvRtY5pr47UmKBm"},{"@type":"CROSSREF","@value":"10.1002/chem.201903443_references_DOI_VEuIWNyNiZ90YvRtY5pr47UmKBm"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.78.1138_references_DOI_VEuIWNyNiZ90YvRtY5pr47UmKBm"}]}