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