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, Loránd | |
dc.date.accessioned | 2017-12-04T05:22:14Z | |
dc.date.available | 2017-12-04T05:22:14Z | |
dc.date.issued | 2017 | |
dc.identifier.citation | Remete, A. M., Nonn, M., Fustero, S., Haukka, M., Fülöp, F., & Kiss, L. (2017). Fluorination of some highly functionalized cycloalkanes: chemoselectivity and substrate dependence. <i>Beilstein Journal of Organic Chemistry</i>, <i>13</i>, 2364-2371. <a href="https://doi.org/10.3762/bjoc.13.233" target="_blank">https://doi.org/10.3762/bjoc.13.233</a> | |
dc.identifier.other | CONVID_27389806 | |
dc.identifier.other | TUTKAID_75896 | |
dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/56087 | |
dc.description.abstract | A study exploring the chemical behavior of some dihydroxylated β-amino ester stereo- and regioisomers, derived from unsaturated
cyclic β-amino acids is described. The nucleophilic fluorinations involving hydroxy–fluorine exchange of some highly functionalized
alicyclic diol derivatives have been carried out in view of selective fluorination, investigating substrate dependence, neighboring
group assistance and chemodifferentiation. | |
dc.language.iso | eng | |
dc.publisher | Beilstein-Institut | |
dc.relation.ispartofseries | Beilstein Journal of Organic Chemistry | |
dc.subject.other | chemoselectivity | |
dc.subject.other | functionalization | |
dc.subject.other | stereoisomers | |
dc.title | Fluorination of some highly functionalized cycloalkanes: chemoselectivity and substrate dependence | |
dc.type | article | |
dc.identifier.urn | URN:NBN:fi:jyu-201711294423 | |
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 | 2017-11-29T13:15:11Z | |
dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
dc.description.reviewstatus | peerReviewed | |
dc.format.pagerange | 2364-2371 | |
dc.relation.issn | 2195-951X | |
dc.relation.numberinseries | 0 | |
dc.relation.volume | 13 | |
dc.type.version | publishedVersion | |
dc.rights.copyright | © 2017 Remete et al.; licensee Beilstein-Institut. This is an open access article distributed under the terms of a Creative Commons License. | |
dc.rights.accesslevel | openAccess | fi |
dc.subject.yso | aminohapot | |
dc.subject.yso | fluori | |
dc.subject.yso | isomeria | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p9530 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p16439 | |
jyx.subject.uri | http://www.yso.fi/onto/yso/p10129 | |
dc.rights.url | https://creativecommons.org/licenses/by/4.0/ | |
dc.relation.doi | 10.3762/bjoc.13.233 | |
dc.type.okm | A1 | |