dc.contributor.author | Angelucci, Francesco | |
dc.contributor.author | Cirillo, Davide | |
dc.contributor.author | Bjørsvik, Hans-René | |
dc.date.accessioned | 2023-01-23T12:42:59Z | |
dc.date.available | 2023-01-23T12:42:59Z | |
dc.date.created | 2022-09-14T18:03:37Z | |
dc.date.issued | 2022 | |
dc.identifier.issn | 1434-193X | |
dc.identifier.uri | https://hdl.handle.net/11250/3045327 | |
dc.description.abstract | A selective and high-rate Ru-catalyzed cross-metathesis reaction of alkenes with vinylimidazole is disclosed. Cross-metathesis is known to operate less efficiently on N-heterocycles, but through optimization by means of statistical experimental design and multiple regression, optimal reaction conditions were identified that allowed for consistent high-yields without the need of overly complicated set-ups or additives. The method was tested on a series of terminal alkene reagents with a variety of different functional groups and it provides the corresponding target molecules in good to high yields. | en_US |
dc.language.iso | eng | en_US |
dc.publisher | Wiley | en_US |
dc.rights | Navngivelse 4.0 Internasjonal | * |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/deed.no | * |
dc.title | Imidazole Backbone Functionalization with Olefin Cross-Metathesis | en_US |
dc.type | Journal article | en_US |
dc.type | Peer reviewed | en_US |
dc.description.version | publishedVersion | en_US |
dc.rights.holder | Copyright 2022 the authors | en_US |
dc.source.articlenumber | e202200437 | en_US |
cristin.ispublished | true | |
cristin.fulltext | original | |
cristin.qualitycode | 1 | |
dc.identifier.doi | 10.1002/ejoc.202200437 | |
dc.identifier.cristin | 2051775 | |
dc.source.journal | European Journal of Organic Chemistry | en_US |
dc.identifier.citation | European Journal of Organic Chemistry. 2022, 2022 (22), e202200437. | en_US |
dc.source.volume | 2022 | en_US |
dc.source.issue | 22 | en_US |