[3+2]-Cycloadditions of N-Cyano Sulfoximines with 1,3-Dipoles

Krauskopf, Felix; Truong, Khai-Nghi; Rissanen, Kari; Bolm, Carsten

doi:10.1002/ejoc.202000335

dc.contributor.author	Krauskopf, Felix
dc.contributor.author	Truong, Khai-Nghi
dc.contributor.author	Rissanen, Kari
dc.contributor.author	Bolm, Carsten
dc.date.accessioned	2020-04-30T09:30:04Z
dc.date.available	2020-04-30T09:30:04Z
dc.date.issued	2020
dc.identifier.citation	Krauskopf, 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.other	CONVID_35119908
dc.identifier.uri	https://jyx.jyu.fi/handle/123456789/68790
dc.description.abstract	Involving 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.mimetype	application/pdf
dc.language	eng
dc.language.iso	eng
dc.publisher	Wiley-VCH Verlag
dc.relation.ispartofseries	European Journal of Organic Chemistry
dc.rights	CC BY 4.0
dc.subject.other	betaine
dc.subject.other	cycloaddition
dc.subject.other	1,3-dipole
dc.subject.other	oxadiazole
dc.subject.other	sulfoximine
dc.subject.other	triazole
dc.title	[3+2]-Cycloadditions of N-Cyano Sulfoximines with 1,3-Dipoles
dc.type	article
dc.identifier.urn	URN:NBN:fi:jyu-202004302998
dc.contributor.laitos	Kemian laitos	fi
dc.contributor.laitos	Department of Chemistry	en
dc.contributor.oppiaine	Orgaaninen kemia	fi
dc.contributor.oppiaine	Organic Chemistry	en
dc.type.uri	http://purl.org/eprint/type/JournalArticle
dc.type.coar	http://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatus	peerReviewed
dc.format.pagerange	2761-2765
dc.relation.issn	1434-193X
dc.relation.numberinseries	18
dc.relation.volume	20
dc.type.version	publishedVersion
dc.rights.copyright	© 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.
dc.rights.accesslevel	openAccess	fi
dc.subject.yso	betaiini
dc.subject.yso	orgaaniset yhdisteet
dc.subject.yso	bioaktiiviset yhdisteet
dc.format.content	fulltext
jyx.subject.uri	http://www.yso.fi/onto/yso/p9529
jyx.subject.uri	http://www.yso.fi/onto/yso/p3841
jyx.subject.uri	http://www.yso.fi/onto/yso/p28433
dc.rights.url	https://creativecommons.org/licenses/by/4.0/
dc.relation.doi	10.1002/ejoc.202000335
jyx.fundinginformation	We 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
dc.type.okm	A1

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