| dc.contributor.author | Vijayan, Ajesh | |
| dc.contributor.author | Baiju, T. V. | |
| dc.contributor.author | Jijy, E. | |
| dc.contributor.author | Prakash, Praveen | |
| dc.contributor.author | Shimi, M. | |
| dc.contributor.author | Joseph, Nayana | |
| dc.contributor.author | Pihko, Petri | |
| dc.contributor.author | Varughese, Sunil | |
| dc.contributor.author | Radhakrishnan, K. V. | |
| dc.date.accessioned | 2016-07-01T10:05:50Z | |
| dc.date.available | 2018-05-12T21:45:07Z | |
| dc.date.issued | 2016 | |
| dc.identifier.citation | Vijayan, A., Baiju, T. V., Jijy, E., Prakash, P., Shimi, M., Joseph, N., Pihko, P., Varughese, S., & Radhakrishnan, K. V. (2016). An easy access to fused chromanones via rhodium catalyzed oxidative coupling of salicylaldehydes with heterobicyclic olefins. <i>Tetrahedron</i>, <i>72</i>(27-28), 4007-4015. <a href="https://doi.org/10.1016/j.tet.2016.05.031" target="_blank">https://doi.org/10.1016/j.tet.2016.05.031</a> | |
| dc.identifier.other | CONVID_25704958 | |
| dc.identifier.other | TUTKAID_70025 | |
| dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/50682 | |
| dc.description.abstract | Herein we describe a detailed study on the rhodium catalyzed oxidative coupling of salicylaldehydes with heterobicyclic olefins such as diazabicyclic olefins and urea-derived bicyclic olefins. The developed method provides an ideal route to fused chromanone systems in a single synthetic step. Moreover, the scope of this methodology was extended to different oxa/aza-bridged bicyclic urea derivatives. | |
| dc.language.iso | eng | |
| dc.publisher | Pergamon | |
| dc.relation.ispartofseries | Tetrahedron | |
| dc.subject.other | chromanone | |
| dc.subject.other | rhodium catalyzed | |
| dc.subject.other | diazabicyclic olefins | |
| dc.subject.other | urea derived bicyclic olefins | |
| dc.subject.other | salicylaldehyde | |
| dc.title | An easy access to fused chromanones via rhodium catalyzed oxidative coupling of salicylaldehydes with heterobicyclic olefins | |
| dc.type | article | |
| dc.identifier.urn | URN:NBN:fi:jyu-201607013429 | |
| dc.contributor.laitos | Kemian laitos | fi |
| dc.contributor.laitos | Department of Chemistry | en |
| dc.contributor.oppiaine | Orgaaninen kemia | fi |
| dc.contributor.oppiaine | Organic Chemistry | en |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
| dc.date.updated | 2016-07-01T09:15:06Z | |
| dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
| dc.description.reviewstatus | peerReviewed | |
| dc.format.pagerange | 4007-4015 | |
| dc.relation.issn | 0040-4020 | |
| dc.relation.numberinseries | 27-28 | |
| dc.relation.volume | 72 | |
| dc.type.version | acceptedVersion | |
| dc.rights.copyright | © 2016 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.relation.doi | 10.1016/j.tet.2016.05.031 | |
| dc.type.okm | A1 | |
