Synthesis of novel fluorinated building blocks via halofluorination and related reactions

Remete, Attila Márió; Novák, Tamás T.; Nonn, Melinda; Haukka, Matti; Fülöp, Ferenc; Kiss, Loránd

doi:10.3762/bjoc.16.208

dc.contributor.author	Remete, Attila Márió
dc.contributor.author	Novák, Tamás T.
dc.contributor.author	Nonn, Melinda
dc.contributor.author	Haukka, Matti
dc.contributor.author	Fülöp, Ferenc
dc.contributor.author	Kiss, Loránd
dc.date.accessioned	2020-11-26T12:31:28Z
dc.date.available	2020-11-26T12:31:28Z
dc.date.issued	2020
dc.identifier.citation	Remete, A. M., Novák, T. T., Nonn, M., Haukka, M., Fülöp, F., & Kiss, L. (2020). Synthesis of novel fluorinated building blocks via halofluorination and related reactions. <i>Beilstein Journal of Organic Chemistry</i>, <i>16</i>, 2562-2575. <a href="https://doi.org/10.3762/bjoc.16.208" target="_blank">https://doi.org/10.3762/bjoc.16.208</a>
dc.identifier.other	CONVID_47123580
dc.identifier.uri	https://jyx.jyu.fi/handle/123456789/72834
dc.description.abstract	A study exploring halofluorination and fluoroselenation of some cyclic olefins, such as diesters, imides, and lactams with varied functionalization patterns and different structural architectures is described. The synthetic methodologies were based on electrophilic activation through halonium ions of the ring olefin bonds, followed by nucleophilic fluorination with Deoxo-Fluor®. The fluorine-containing products thus obtained were subjected to elimination reactions, yielding various fluorine-containing small-molecular entities.	en
dc.format.mimetype	application/pdf
dc.language	eng
dc.language.iso	eng
dc.publisher	Beilstein-Institut zur Förderung der Chemischen Wissenschaften
dc.relation.ispartofseries	Beilstein Journal of Organic Chemistry
dc.rights	CC BY 4.0
dc.subject.other	fluorine
dc.subject.other	fluoroselenation
dc.subject.other	functionalization
dc.subject.other	halofluorination
dc.subject.other	stereocontrol
dc.title	Synthesis of novel fluorinated building blocks via halofluorination and related reactions
dc.type	article
dc.identifier.urn	URN:NBN:fi:jyu-202011266800
dc.contributor.laitos	Kemian laitos	fi
dc.contributor.laitos	Department of Chemistry	en
dc.contributor.oppiaine	Epäorgaaninen kemia	fi
dc.contributor.oppiaine	Epäorgaaninen ja analyyttinen kemia	fi
dc.contributor.oppiaine	Inorganic Chemistry	en
dc.contributor.oppiaine	Inorganic and Analytical 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	2562-2575
dc.relation.issn	2195-951X
dc.relation.volume	16
dc.type.version	publishedVersion
dc.rights.copyright	© 2020 Remete et al.; licensee Beilstein-Institut
dc.rights.accesslevel	openAccess	fi
dc.subject.yso	kemiallinen synteesi
dc.subject.yso	orgaaniset yhdisteet
dc.subject.yso	fluori
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/p16439
dc.rights.url	https://creativecommons.org/licenses/by/4.0/
dc.relation.doi	10.3762/bjoc.16.208
jyx.fundinginformation	We are grateful to the Hungarian Research Foundation (NKFIH No K 119282) for financial support. Fnancial support of the GINOP-2.3.2-15-2016-00038 project is also acknowledged. This research was supported by the EU-funded Hungarian grant EFOP-3.6.1-16-2016-00008. The Ministry of Human Capacities, Hungary (grant 20391-3/2018/FEKUSTRAT) is also acknowledged.
dc.type.okm	A1

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Synthesis of novel fluorinated building blocks via halofluorination and related reactions

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