dc.contributor.author | Fekete, Beáta | |
dc.contributor.author | Palkó, Márta | |
dc.contributor.author | Haukka, Matti | |
dc.contributor.author | Fülöp, Ferenc | |
dc.date.accessioned | 2017-05-03T06:34:02Z | |
dc.date.available | 2017-05-03T06:34:02Z | |
dc.date.issued | 2017 | |
dc.identifier.citation | Fekete, B., Palkó, M., Haukka, M., & Fülöp, F. (2017). Synthesis of Pyrrolo[1,2-a]pyrimidine Enantiomers via Domino Ring-Closure followed by Retro Diels-Alder Protocol. <i>Molecules</i>, <i>22</i>(4), Article 613. <a href="https://doi.org/10.3390/molecules22040613" target="_blank">https://doi.org/10.3390/molecules22040613</a> | |
dc.identifier.other | CONVID_26967332 | |
dc.identifier.other | TUTKAID_73587 | |
dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/53750 | |
dc.description.abstract | From 2-aminonorbornene hydroxamic acids, a simple and efficient method for the
preparation of pyrrolo[1,2-a]pyrimidine enantiomers is reported. The synthesis is based on domino
ring-closure followed by microwave-induced retro Diels-Alder (RDA) protocols, where the chirality
of the desired products is transferred from norbornene derivatives. The stereochemistry of the
synthesized compounds was proven by X-ray crystallography. The absolute configuration of the
product is determined by the configuration of the starting amino hydroxamic acid. | |
dc.language.iso | eng | |
dc.publisher | MDPI | |
dc.relation.ispartofseries | Molecules | |
dc.subject.other | N-heterocycles | |
dc.subject.other | domino reactions | |
dc.subject.other | hydroxamic acid | |
dc.subject.other | microwave chemistry | |
dc.subject.other | retro Diels-Alder reaction | |
dc.title | Synthesis of Pyrrolo[1,2-a]pyrimidine Enantiomers via Domino Ring-Closure followed by Retro Diels-Alder Protocol | |
dc.type | article | |
dc.identifier.urn | URN:NBN:fi:jyu-201704242055 | |
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 | 2017-04-24T12:15:12Z | |
dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
dc.description.reviewstatus | peerReviewed | |
dc.relation.issn | 1420-3049 | |
dc.relation.numberinseries | 4 | |
dc.relation.volume | 22 | |
dc.type.version | publishedVersion | |
dc.rights.copyright | © the Authors, 2017. This is an open access article distributed under the Creative Commons Attribution License. | |
dc.rights.accesslevel | openAccess | fi |
dc.rights.url | https://creativecommons.org/licenses/by/4.0/ | |
dc.relation.doi | 10.3390/molecules22040613 | |
dc.type.okm | A1 | |