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dc.contributor.authorKrauskopf, Felix
dc.contributor.authorTruong, Khai-Nghi
dc.contributor.authorRissanen, Kari
dc.contributor.authorBolm, Carsten
dc.date.accessioned2020-04-30T09:30:04Z
dc.date.available2020-04-30T09:30:04Z
dc.date.issued2020
dc.identifier.citationKrauskopf, F., Truong, K.-N., Rissanen, K., & Bolm, C. (2020). [3+2]-Cycloadditions of N-Cyano Sulfoximines with 1,3-Dipoles. <i>European Journal of Organic Chemistry</i>, <i>20</i>(18), 2761-2765. <a href="https://doi.org/10.1002/ejoc.202000335" target="_blank">https://doi.org/10.1002/ejoc.202000335</a>
dc.identifier.otherCONVID_35119908
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/68790
dc.description.abstractInvolving the cyano group of N‐cyano sulfoximines in [3+2]‐cycloaddition reactions with 1,3‐dipoles provides practical routes for the construction of 5‐membered heterocycles bearing sulfoximinoyl moieties. An ytterbium‐catalyzed cycloaddition utilizing hydrazonoyl chlorides was developed, as well as a reaction involving imidoyl chlorides proceeding without the aid of a catalyst. Following these protocols, a range of sulfoximines with N‐1,2,4‐triazolyl and N‐1,2,4‐oxadiazolyl substituents was prepared.en
dc.format.mimetypeapplication/pdf
dc.languageeng
dc.language.isoeng
dc.publisherWiley-VCH Verlag
dc.relation.ispartofseriesEuropean Journal of Organic Chemistry
dc.rightsCC BY 4.0
dc.subject.otherbetaine
dc.subject.othercycloaddition
dc.subject.other1,3-dipole
dc.subject.otheroxadiazole
dc.subject.othersulfoximine
dc.subject.othertriazole
dc.title[3+2]-Cycloadditions of N-Cyano Sulfoximines with 1,3-Dipoles
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-202004302998
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.description.reviewstatuspeerReviewed
dc.format.pagerange2761-2765
dc.relation.issn1434-193X
dc.relation.numberinseries18
dc.relation.volume20
dc.type.versionpublishedVersion
dc.rights.copyright© 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.
dc.rights.accesslevelopenAccessfi
dc.subject.ysobetaiini
dc.subject.ysoorgaaniset yhdisteet
dc.subject.ysobioaktiiviset yhdisteet
dc.format.contentfulltext
jyx.subject.urihttp://www.yso.fi/onto/yso/p9529
jyx.subject.urihttp://www.yso.fi/onto/yso/p3841
jyx.subject.urihttp://www.yso.fi/onto/yso/p28433
dc.rights.urlhttps://creativecommons.org/licenses/by/4.0/
dc.relation.doi10.1002/ejoc.202000335
jyx.fundinginformationWe are grateful to the Alexander von Humboldt Foundation for support of K.R. (AvH research award) and thank S. Huda, A. Krohmer, and F. Brosge (all RWTH Aachen University) for their practical work and assistance in preparing starting materials


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