{"@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/1363670320757181184.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1002/asia.200900458"}},{"identifier":{"@type":"URI","@value":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fasia.200900458"}},{"identifier":{"@type":"URI","@value":"https://aces.onlinelibrary.wiley.com/doi/pdf/10.1002/asia.200900458"}}],"dc:title":[{"@value":"Recent Advances in Multicatalyst Promoted Asymmetric Tandem Reactions"}],"description":[{"type":"abstract","notation":[{"@value":"<jats:title>Abstract</jats:title><jats:p>Multicatalyst promoted asymmetric tandem reactions have emerged as a powerful strategy to improve the synthetic efficiency. It enables the synthesis of complex molecules with high selectivity from simple starting materials in an almost biomimetic‐like way. The use of multiple catalyst systems can enlarge the substrate and reaction scope for the reaction design, improve the reactivity, and benefit the control of selectivity. In this Focus Review, the current achievement of this promising field is discussed, including the advantages and difficulties of this research, and the strategies applied to address these problems.</jats:p>"}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1383670320757181184","@type":"Researcher","foaf:name":[{"@value":"Jian Zhou"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"18614728"},{"@type":"EISSN","@value":"1861471X"}],"prism:publicationName":[{"@value":"Chemistry – An Asian Journal"}],"dc:publisher":[{"@value":"Wiley"}],"prism:publicationDate":"2010-02-22","prism:volume":"5","prism:number":"3","prism:startingPage":"422","prism:endingPage":"434"},"reviewed":"false","dc:rights":["http://onlinelibrary.wiley.com/termsAndConditions#vor"],"url":[{"@id":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fasia.200900458"},{"@id":"https://aces.onlinelibrary.wiley.com/doi/pdf/10.1002/asia.200900458"}],"createdAt":"2010-01-28","modifiedAt":"2025-10-08","relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1360002216875586688","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Dynamic asymmetric organocatalysis: cooperative effects of weak interactions and conformational flexibility in asymmetric organocatalysts"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004233611718400","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Integration of aerobic oxidation and intramolecular asymmetric aza-Friedel–Crafts reactions with a chiral bifunctional heterogeneous catalyst"}]},{"@id":"https://cir.nii.ac.jp/crid/1360283691154816384","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Asymmetric synthesis of highly functionalized γ-lactams through an organocatalytic aza-Michael–Michael reaction cascade using fumaric acid amide esters as multi-reactive substrates"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285708107799808","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Asymmetric α-Allylation of α-Substituted β-Ketoesters with Allyl Alcohols"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285708118506624","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"One-Pot Catalysis Using a Chiral Iridium Complex/Brønsted Base: Catalytic Asymmetric Synthesis of Catalponol"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285708125753856","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Chiral Ligand-Modified Metal Nanoparticles as Unique Catalysts for Asymmetric C–C Bond-Forming Reactions: How Are Active Species Generated?"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285708141287168","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Sequence-Regulated Polymers via Living Radical Polymerization: From Design to Properties and Functions"}]},{"@id":"https://cir.nii.ac.jp/crid/1360565164377079808","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Relay Catalysis Using a Rhodium Complex/Chiral Brønsted Acid Binary System: Enantioselective Reduction of a Carbonyl Ylide as the Reactive Intermediate"}]},{"@id":"https://cir.nii.ac.jp/crid/1360565166845883776","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Pot economy and one-pot synthesis"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567183166245376","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Polymer-Incarcerated Gold−Palladium Nanoclusters with Boron on Carbon: A Mild and Efficient Catalyst for the Sequential Aerobic Oxidation−Michael Addition of 1,3-Dicarbonyl Compounds to Allylic Alcohols"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567183167217536","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Mechanistic Studies of Highly Enantio- and Diastereoselective Aza-Petasis–Ferrier Rearrangement Catalyzed by Chiral Phosphoric Acid"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567183523408384","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Tandem catalysis in domino olefin cross-metathesis/intramolecular oxa-conjugate cyclization: concise synthesis of 2,6-cis-substituted tetrahydropyran derivatives"}]},{"@id":"https://cir.nii.ac.jp/crid/1360846639354524928","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Chiral Copper(II) Phosphate Catalyzed Enantioselective Synthesis of Isochromene Derivatives by Sequential Intramolecular Cyclization and Asymmetric Transfer Hydrogenation of <i>o</i>‐Alkynylacetophenones"}]},{"@id":"https://cir.nii.ac.jp/crid/1360846641588510720","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Sequence-Regulated Copolymers via Tandem Catalysis of Living Radical Polymerization and In Situ Transesterification"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848654917841920","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Oxidative Esterification, Thioesterification, and Amidation of Aldehydes by a Two‐Component Organocatalyst System Using a Chiral N‐Heterocyclic Carbene and Redox‐Active Riboflavin"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848658179408896","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Peptide/Laccase Cocatalyzed Asymmetric α-Oxyamination of Aldehydes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848661052302464","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Oxidative transformation of N-substituted 2-aminophenols to 2-substituted benzoxazoles catalyzed by polymer-incarcerated and carbon-stabilized platinum nanoclusters"}]},{"@id":"https://cir.nii.ac.jp/crid/1390001205341603072","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Enantioselective Transformations Catalyzed by Chiral Brønsted Acids"},{"@language":"ja","@value":"キラルBrønsted酸を用いた不斉触媒反応"},{"@language":"ja-Kana","@value":"キラル Brønstedサン オ モチイタ フセイ ショクバイ ハンノウ"},{"@value":"Enantioselective Transformations Catalyzed by Chiral Br^|^oslash;nsted Acids"}]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1002/asia.200900458"},{"@type":"CROSSREF","@value":"10.1039/c2cc31846f_references_DOI_BEteSPMrNBerHckHg2xf9YgUR3q"},{"@type":"CROSSREF","@value":"10.1039/c6sc03849b_references_DOI_BEteSPMrNBerHckHg2xf9YgUR3q"},{"@type":"CROSSREF","@value":"10.1021/ja211436n_references_DOI_BEteSPMrNBerHckHg2xf9YgUR3q"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.71.480_references_DOI_BEteSPMrNBerHckHg2xf9YgUR3q"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.5b02480_references_DOI_BEteSPMrNBerHckHg2xf9YgUR3q"},{"@type":"CROSSREF","@value":"10.1002/anie.201107805_references_DOI_BEteSPMrNBerHckHg2xf9YgUR3q"},{"@type":"CROSSREF","@value":"10.1039/c5sc02913a_references_DOI_BEteSPMrNBerHckHg2xf9YgUR3q"},{"@type":"CROSSREF","@value":"10.1039/c2ob26189h_references_DOI_BEteSPMrNBerHckHg2xf9YgUR3q"},{"@type":"CROSSREF","@value":"10.1021/bk-2014-1170.ch017_references_DOI_BEteSPMrNBerHckHg2xf9YgUR3q"},{"@type":"CROSSREF","@value":"10.1021/acs.joc.7b02188_references_DOI_BEteSPMrNBerHckHg2xf9YgUR3q"},{"@type":"CROSSREF","@value":"10.1021/ol2012956_references_DOI_BEteSPMrNBerHckHg2xf9YgUR3q"},{"@type":"CROSSREF","@value":"10.1002/anie.201308303_references_DOI_BEteSPMrNBerHckHg2xf9YgUR3q"},{"@type":"CROSSREF","@value":"10.1002/chem.201100737_references_DOI_BEteSPMrNBerHckHg2xf9YgUR3q"},{"@type":"CROSSREF","@value":"10.1139/v11-161_references_DOI_BEteSPMrNBerHckHg2xf9YgUR3q"},{"@type":"CROSSREF","@value":"10.1021/acscatal.6b02446_references_DOI_BEteSPMrNBerHckHg2xf9YgUR3q"},{"@type":"CROSSREF","@value":"10.1021/ja110142y_references_DOI_BEteSPMrNBerHckHg2xf9YgUR3q"},{"@type":"CROSSREF","@value":"10.1021/ja5017206_references_DOI_BEteSPMrNBerHckHg2xf9YgUR3q"},{"@type":"CROSSREF","@value":"10.1016/j.tetlet.2011.12.114_references_DOI_BEteSPMrNBerHckHg2xf9YgUR3q"}]}