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dc.contributor.authorWu, Peng
dc.contributor.authorWard, Jas S.
dc.contributor.authorRissanen, Kari
dc.contributor.authorBolm, Carsten
dc.date.accessioned2023-02-27T11:02:10Z
dc.date.available2023-02-27T11:02:10Z
dc.date.issued2023
dc.identifier.citationWu, P., Ward, J. S., Rissanen, K., & Bolm, C. (2023). Cyclic Sulfoximine and Sulfonimidamide Derivatives by Copper‐Catalyzed Cross‐Coupling Reactions with Elemental Sulfur. <i>Advanced Synthesis and Catalysis</i>, <i>365</i>(4), 522-526. <a href="https://doi.org/10.1002/adsc.202201408" target="_blank">https://doi.org/10.1002/adsc.202201408</a>
dc.identifier.otherCONVID_177039584
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/85660
dc.description.abstractCopper-catalyzed cross-coupling reactions of α-bromoaryl NH-sulfoximines with elemental sulfur lead to benzo[d][1,3,2]dithiazole-1-oxides, which represent a new class of three-dimensional heterocycles. The reactions proceed under mild conditions showing good functional group and heterocycle tolerance. By imination/oxidation, the initial cross-coupling products can be converted to unprecedented cyclic sulfonimidamides derivatives. Furthermore, a seven-membered heterocycle was obtained by a ruthenium-catalyzed ring-expansion with ethyl propiolate.en
dc.format.mimetypeapplication/pdf
dc.language.isoeng
dc.publisherWiley
dc.relation.ispartofseriesAdvanced Synthesis and Catalysis
dc.rightsCC BY 4.0
dc.subject.othercopper catalysis
dc.subject.otherelemental sulfur
dc.subject.othersulfoximines
dc.subject.othersulfonimidamides
dc.subject.othercross-coupling reactions
dc.titleCyclic Sulfoximine and Sulfonimidamide Derivatives by Copper‐Catalyzed Cross‐Coupling Reactions with Elemental Sulfur
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202302271922
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineOrgaaninen kemiafi
dc.contributor.oppiaineOrganic Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerange522-526
dc.relation.issn1615-4150
dc.relation.numberinseries4
dc.relation.volume365
dc.type.versionpublishedVersion
dc.rights.copyright© 2023 The Authors. Advanced Synthesis & Catalysis published by Wiley-VCH GmbH
dc.rights.accesslevelopenAccessfi
dc.subject.ysokatalyysi
dc.subject.ysorikki
dc.subject.ysokupari
dc.subject.ysorikkiyhdisteet
dc.subject.ysokatalyytit
dc.subject.ysoheterosykliset yhdisteet
dc.subject.ysokemiallinen synteesi
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p8704
jyx.subject.urihttp://www.yso.fi/onto/yso/p12305
jyx.subject.urihttp://www.yso.fi/onto/yso/p19074
jyx.subject.urihttp://www.yso.fi/onto/yso/p5731
jyx.subject.urihttp://www.yso.fi/onto/yso/p15480
jyx.subject.urihttp://www.yso.fi/onto/yso/p38837
jyx.subject.urihttp://www.yso.fi/onto/yso/p8468
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1002/adsc.202201408
jyx.fundinginformationP. W. is grateful to the China Scholarship Council (CSC) for a predoctoral stipend, and we acknowledge the Alexander von Humboldt Foundation for support of K. R. (AvH research award). Open Access funding enabled and organized by Projekt DEAL.
dc.type.okmA1


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