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dc.contributor.authorLiu, Qiang
dc.contributor.authorChen, Xiang-Yu
dc.contributor.authorPuttreddy, Rakesh
dc.contributor.authorRissanen, Kari
dc.contributor.authorEnders, Dieter
dc.date.accessioned2019-01-07T08:10:00Z
dc.date.available2019-11-05T22:35:16Z
dc.date.issued2018
dc.identifier.citationLiu, Q., Chen, X.-Y., Puttreddy, R., Rissanen, K., & Enders, D. (2018). N-Heterocyclic Carbene Catalyzed Quadruple Domino Reactions through α,β-Unsaturated Acyl Azolium Intermediates : Asymmetric Synthesis of Cyclopenta[c]chromenones. <i>Angewandte Chemie</i>, <i>57</i>(52), 17100-17103. <a href="https://doi.org/10.1002/anie.201810402" target="_blank">https://doi.org/10.1002/anie.201810402</a>
dc.identifier.otherCONVID_28705064
dc.identifier.otherTUTKAID_79413
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/60922
dc.description.abstractAn N‐heterocyclic carbene catalyzed domino sequence via α,β‐unsaturated acyl azolium intermediates has been developed. This strategy provides a convenient enantioselective route to functionalized tricyclic coumarin derivatives and cyclopentanes. DFT studies and control experiments were performed to gain better insight into the reaction mechanism.fi
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherWiley, VCH Verlag GmbH & Co. KGaA
dc.relation.ispartofseriesAngewandte Chemie
dc.rightsIn Copyright
dc.subject.otherN-heterocyclic carbene
dc.subject.otherdomino reaction
dc.subject.otherchromenone
dc.subject.otherorganocatalysis
dc.subject.otherDFT calculation
dc.titleN-Heterocyclic Carbene Catalyzed Quadruple Domino Reactions through α,β-Unsaturated Acyl Azolium Intermediates : Asymmetric Synthesis of Cyclopenta[c]chromenones
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201812275336
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineKemiafi
dc.contributor.oppiaineOrgaaninen kemiafi
dc.contributor.oppiaineChemistryen
dc.contributor.oppiaineOrganic Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.date.updated2018-12-27T13:15:09Z
dc.description.reviewstatuspeerReviewed
dc.format.pagerange17100-17103
dc.relation.issn1433-7851
dc.relation.numberinseries52
dc.relation.volume57
dc.type.versionacceptedVersion
dc.rights.copyright© 2018 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim
dc.rights.accesslevelopenAccessfi
dc.subject.ysokemiallinen synteesi
dc.subject.ysoorgaaniset yhdisteet
dc.subject.ysokumariinit
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p8468
jyx.subject.urihttp://www.yso.fi/onto/yso/p3841
jyx.subject.urihttp://www.yso.fi/onto/yso/p19317
dc.rights.urlhttp://rightsstatements.org/page/InC/1.0/?language=en
dc.relation.doi10.1002/anie.201810402


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