| dc.contributor.author | Miklós, Ferenc | |
| dc.contributor.author | Bozó, Kristóf | |
| dc.contributor.author | Galla, Zsolt | |
| dc.contributor.author | Haukka, Matti | |
| dc.contributor.author | Fülöp, Ferenc | |
| dc.date.accessioned | 2017-11-07T11:30:00Z | |
| dc.date.available | 2019-10-15T21:35:23Z | |
| dc.date.issued | 2017 | |
| dc.identifier.citation | Miklós, F., Bozó, K., Galla, Z., Haukka, M., & Fülöp, F. (2017). Traceless chirality transfer from a norbornene β-amino acid to pyrimido[2,1-a]isoindole enantiomers. <i>Tetrahedron: Asymmetry</i>, <i>28</i>(10), 1401-1406. <a href="https://doi.org/10.1016/j.tetasy.2017.07.006" target="_blank">https://doi.org/10.1016/j.tetasy.2017.07.006</a> | |
| dc.identifier.other | CONVID_27157142 | |
| dc.identifier.other | TUTKAID_74647 | |
| dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/55787 | |
| dc.description.abstract | The synthesis of two enantiomeric pairs of pyrimidoisoindoles 9a, 9b and 10a, 10b is reported. During a domino ring-closure reaction, followed by cycloreversion, the chirality of diendo-(−)-(1R,2S,3R,4S)-3-aminobicyclo[2.2.1]hept-5-ene-2-carboxamide [(−)-1] was successfully transfered to heterocycles (+)-9a, (+)-10a, (−)-9b, (−)-10b and (−)-10c. | |
| dc.language.iso | eng | |
| dc.publisher | Pergamon Press | |
| dc.relation.ispartofseries | Tetrahedron: Asymmetry | |
| dc.subject.other | heterocycles | |
| dc.title | Traceless chirality transfer from a norbornene β-amino acid to pyrimido[2,1-a]isoindole enantiomers | |
| dc.type | article | |
| dc.identifier.urn | URN:NBN:fi:jyu-201711064142 | |
| 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 | 2017-11-06T13:15:10Z | |
| dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
| dc.description.reviewstatus | peerReviewed | |
| dc.format.pagerange | 1401-1406 | |
| dc.relation.issn | 0957-4166 | |
| dc.relation.numberinseries | 10 | |
| dc.relation.volume | 28 | |
| dc.type.version | acceptedVersion | |
| dc.rights.copyright | © 2017 Elsevier Ltd. This is a final draft version of an article whose final and definitive form has been published by Elsevier. Published in this repository with the kind permission of the publisher. | |
| dc.rights.accesslevel | openAccess | fi |
| dc.subject.yso | kemia | |
| dc.subject.yso | biologia | |
| dc.subject.yso | farmasia | |
| dc.subject.yso | aminohapot | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p1801 | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p1782 | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p5772 | |
| jyx.subject.uri | http://www.yso.fi/onto/yso/p9530 | |
| dc.relation.doi | 10.1016/j.tetasy.2017.07.006 | |
| dc.type.okm | A1 | |
