Synthesis of novel fluorinated building blocks via halofluorination and related reactions
| 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 | research 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.type.publication | article | |
| 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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