N-Heterocyclic Carbene Catalyzed Quadruple Domino Reactions through α,β-Unsaturated Acyl Azolium Intermediates : Asymmetric Synthesis of Cyclopenta[c]chromenones

Liu, Qiang; Chen, Xiang-Yu; Puttreddy, Rakesh; Rissanen, Kari; Enders, Dieter

doi:10.1002/anie.201810402

dc.contributor.author	Liu, Qiang
dc.contributor.author	Chen, Xiang-Yu
dc.contributor.author	Puttreddy, Rakesh
dc.contributor.author	Rissanen, Kari
dc.contributor.author	Enders, Dieter
dc.date.accessioned	2019-01-07T08:10:00Z
dc.date.available	2019-11-05T22:35:16Z
dc.date.issued	2018
dc.identifier.citation	Liu, 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.other	CONVID_28705064
dc.identifier.other	TUTKAID_79413
dc.identifier.uri	https://jyx.jyu.fi/handle/123456789/60922
dc.description.abstract	An 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.mimetype	application/pdf
dc.language.iso	eng
dc.publisher	Wiley, VCH Verlag GmbH & Co. KGaA
dc.relation.ispartofseries	Angewandte Chemie
dc.rights	In Copyright
dc.subject.other	N-heterocyclic carbene
dc.subject.other	domino reaction
dc.subject.other	chromenone
dc.subject.other	organocatalysis
dc.subject.other	DFT calculation
dc.title	N-Heterocyclic Carbene Catalyzed Quadruple Domino Reactions through α,β-Unsaturated Acyl Azolium Intermediates : Asymmetric Synthesis of Cyclopenta[c]chromenones
dc.type	article
dc.identifier.urn	URN:NBN:fi:jyu-201812275336
dc.contributor.laitos	Kemian laitos	fi
dc.contributor.laitos	Department of Chemistry	en
dc.contributor.oppiaine	Kemia	fi
dc.contributor.oppiaine	Orgaaninen kemia	fi
dc.contributor.oppiaine	Chemistry	en
dc.contributor.oppiaine	Organic Chemistry	en
dc.type.uri	http://purl.org/eprint/type/JournalArticle
dc.date.updated	2018-12-27T13:15:09Z
dc.type.coar	http://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatus	peerReviewed
dc.format.pagerange	17100-17103
dc.relation.issn	1433-7851
dc.relation.numberinseries	52
dc.relation.volume	57
dc.type.version	acceptedVersion
dc.rights.copyright	© 2018 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim
dc.rights.accesslevel	openAccess	fi
dc.subject.yso	kemiallinen synteesi
dc.subject.yso	orgaaniset yhdisteet
dc.subject.yso	kumariinit
dc.format.content	fulltext
jyx.subject.uri	http://www.yso.fi/onto/yso/p8468
jyx.subject.uri	http://www.yso.fi/onto/yso/p3841
jyx.subject.uri	http://www.yso.fi/onto/yso/p19317
dc.rights.url	http://rightsstatements.org/page/InC/1.0/?language=en
dc.relation.doi	10.1002/anie.201810402
dc.type.okm	A1

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N-Heterocyclic Carbene Catalyzed Quadruple Domino Reactions through α,β-Unsaturated Acyl Azolium Intermediates : Asymmetric Synthesis of Cyclopenta[c]chromenones

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