5-Carbonyl-1,3-oxazine-2,4-diones from N-Cyanosulfoximines and Meldrum’s Acid Derivatives

Brosge, Felix; Kochs, Johanne,s Florian; Bregu, Mariela; Truong, Khai-Nghi; Rissanen, Kari; Bolm, Carsten

doi:10.1021/acs.orglett.0c02504

dc.contributor.author	Brosge, Felix
dc.contributor.author	Kochs, Johanne,s Florian
dc.contributor.author	Bregu, Mariela
dc.contributor.author	Truong, Khai-Nghi
dc.contributor.author	Rissanen, Kari
dc.contributor.author	Bolm, Carsten
dc.date.accessioned	2020-12-22T06:34:03Z
dc.date.available	2020-12-22T06:34:03Z
dc.date.issued	2020
dc.identifier.citation	Brosge, F., Kochs, J., Bregu, M., Truong, K.-N., Rissanen, K., & Bolm, C. (2020). 5-Carbonyl-1,3-oxazine-2,4-diones from N-Cyanosulfoximines and Meldrum’s Acid Derivatives. <i>Organic Letters</i>, <i>22</i>(16), 6667-6670. <a href="https://doi.org/10.1021/acs.orglett.0c02504" target="_blank">https://doi.org/10.1021/acs.orglett.0c02504</a>
dc.identifier.other	CONVID_41689181
dc.identifier.uri	https://jyx.jyu.fi/handle/123456789/73362
dc.description.abstract	At elevated temperatures, N-cyanosulfoximines react with Meldrum’s acid derivatives to give sulfoximines with N-bound 5-carbonyl-1,3-oxazine-2,4-dione groups. A representative product was characterized by single-crystal X-ray structure analysis. The product formation involves an unexpected molecular reorientation requiring several sequential bond-forming and -cleaving processes.	en
dc.format.mimetype	application/pdf
dc.language	eng
dc.language.iso	eng
dc.publisher	American Chemical Society (ACS)
dc.relation.ispartofseries	Organic Letters
dc.rights	In Copyright
dc.subject.other	reaction products
dc.subject.other	cyclization
dc.subject.other	crystal structure
dc.subject.other	addition reactions
dc.subject.other	chemical reactions
dc.title	5-Carbonyl-1,3-oxazine-2,4-diones from N-Cyanosulfoximines and Meldrum’s Acid Derivatives
dc.type	research article
dc.identifier.urn	URN:NBN:fi:jyu-202012227305
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	6667-6670
dc.relation.issn	1523-7060
dc.relation.numberinseries	16
dc.relation.volume	22
dc.type.version	acceptedVersion
dc.rights.copyright	© 2020 American Chemical Society
dc.rights.accesslevel	openAccess	fi
dc.type.publication	article
dc.subject.yso	orgaaniset yhdisteet
dc.subject.yso	kemialliset reaktiot
dc.subject.yso	typpiyhdisteet
dc.subject.yso	rikkiyhdisteet
dc.subject.yso	kemiallinen synteesi
dc.format.content	fulltext
jyx.subject.uri	http://www.yso.fi/onto/yso/p3841
jyx.subject.uri	http://www.yso.fi/onto/yso/p3658
jyx.subject.uri	http://www.yso.fi/onto/yso/p640
jyx.subject.uri	http://www.yso.fi/onto/yso/p5731
jyx.subject.uri	http://www.yso.fi/onto/yso/p8468
dc.rights.url	http://rightsstatements.org/page/InC/1.0/?language=en
dc.relation.doi	10.1021/acs.orglett.0c02504
dc.type.okm	A1

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