Fluorine-containing functionalized cyclopentene scaffolds through ring contraction and deoxofluorination of various substituted cyclohexenes

Remete, Attila Márió; Nonn, Melinda; Fustero, Santos; Haukka, Matti; Fülöp, Ferenc; Kiss, Lorand

doi:10.1002/ejoc.201800057

dc.contributor.author	Remete, Attila Márió
dc.contributor.author	Nonn, Melinda
dc.contributor.author	Fustero, Santos
dc.contributor.author	Haukka, Matti
dc.contributor.author	Fülöp, Ferenc
dc.contributor.author	Kiss, Lorand
dc.date.accessioned	2018-08-06T07:58:02Z
dc.date.available	2019-02-14T22:35:18Z
dc.date.issued	2018
dc.identifier.citation	Remete, A. M., Nonn, M., Fustero, S., Haukka, M., Fülöp, F., & Kiss, L. (2018). Fluorine-containing functionalized cyclopentene scaffolds through ring contraction and deoxofluorination of various substituted cyclohexenes. <i>European Journal of Organic Chemistry</i>, <i>2018</i>(27-28), 3735-3742. <a href="https://doi.org/10.1002/ejoc.201800057" target="_blank">https://doi.org/10.1002/ejoc.201800057</a>
dc.identifier.other	CONVID_27893159
dc.identifier.other	TUTKAID_76763
dc.identifier.uri	https://jyx.jyu.fi/handle/123456789/59099
dc.description.abstract	The fluorination of some highly‐functionalized cyclopentene derivatives, obtained from various substituted cyclohexenes through a ring‐opening/ring‐contraction procedure, has been investigated. The transformations were found to be highly substrate dependent, and led to the formation of various functionalized alicyclic compounds or heterocycles containing allyl difluoride or vinyl fluoride moieties.	fi
dc.format.mimetype	application/pdf
dc.language.iso	eng
dc.publisher	Wiley-VCH
dc.relation.ispartofseries	European Journal of Organic Chemistry
dc.rights	In Copyright
dc.subject.other	ring contraction
dc.subject.other	aldol reaction
dc.subject.other	stereoselectivity
dc.title	Fluorine-containing functionalized cyclopentene scaffolds through ring contraction and deoxofluorination of various substituted cyclohexenes
dc.type	article
dc.identifier.urn	URN:NBN:fi:jyu-201807233627
dc.contributor.laitos	Kemian laitos	fi
dc.contributor.laitos	Department of Chemistry	en
dc.contributor.oppiaine	Epäorgaaninen ja analyyttinen kemia	fi
dc.contributor.oppiaine	Inorganic and Analytical Chemistry	en
dc.type.uri	http://purl.org/eprint/type/JournalArticle
dc.date.updated	2018-07-23T06:15:14Z
dc.type.coar	http://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatus	peerReviewed
dc.format.pagerange	3735-3742
dc.relation.issn	1434-193X
dc.relation.numberinseries	27-28
dc.relation.volume	2018
dc.type.version	acceptedVersion
dc.rights.copyright	© 2018 WILEY.
dc.rights.accesslevel	openAccess	fi
dc.subject.yso	orgaaniset yhdisteet
dc.subject.yso	fluoridit
dc.subject.yso	fluori
dc.subject.yso	aminohapot
dc.format.content	fulltext
jyx.subject.uri	http://www.yso.fi/onto/yso/p3841
jyx.subject.uri	http://www.yso.fi/onto/yso/p7109
jyx.subject.uri	http://www.yso.fi/onto/yso/p16439
jyx.subject.uri	http://www.yso.fi/onto/yso/p9530
dc.rights.url	http://rightsstatements.org/page/InC/1.0/?language=en
dc.relation.doi	10.1002/ejoc.201800057
dc.type.okm	A1

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Synthesis of novel fluorinated building blocks via halofluorination and related reactions ﻿

Stereocontrolled synthesis of fluorine-containing piperidine γ-amino acid derivatives ﻿

Fluorination of some highly functionalized cycloalkanes: chemoselectivity and substrate dependence ﻿

[3+2] Cycloaddition Reaction for the Stereoselective Synthesis of a New Spirooxindole Compound Grafted Imidazo[2,1-b]thiazole Scaffold : Crystal Structure and Computational Study ﻿

Design, Construction, and Characterization of a New Regioisomer and Diastereomer Material Based on the Spirooxindole Scaffold Incorporating a Sulphone Function ﻿

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