Please use this identifier to cite or link to this item:
https://hdl.handle.net/1889/5399
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.advisor | Camedda, Nicola Camedda | - |
dc.contributor.author | Camedda, Nicola | - |
dc.date.accessioned | 2023-06-22T14:10:53Z | - |
dc.date.available | 2023-06-22T14:10:53Z | - |
dc.date.issued | 2023 | - |
dc.identifier.uri | https://hdl.handle.net/1889/5399 | - |
dc.description.abstract | The Diels-Alder reaction is among one of the most powerful chemical transformation for making cyclohexene frameworks. However during the last century the understanding of steric and electronic effects occuring in thsi reaction increased a lot an many variants have been developed. One of those is the Dehydro-Diels-Alder reaction. The thesis will focus on the history of these reactions and projects able to reproduce them in mild conditions. | en_US |
dc.language.iso | Inglese | en_US |
dc.publisher | Università degli studi di Parma. Dipartimento di Scienze matematiche, fisiche e informatiche | en_US |
dc.relation.ispartofseries | Dottorato di ricerca in Scienze chimiche | en_US |
dc.rights | © Nicola Camedda, 2023 | en_US |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.subject | Diels-Alder | en_US |
dc.title | Catalytic strategies to trigger challenging Diels-Alder cyclisations under mild conditions | en_US |
dc.type | Doctoral thesis | en_US |
dc.subject.miur | CHIM/06 | en_US |
dc.rights.license | Attribution-NonCommercial-NoDerivatives 4.0 Internazionale | * |
Appears in Collections: | Scienze chimiche. Tesi di dottorato |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
TESI DI DOTTORATO Camedda-firmata.pdf Until 2024-06-01 | 7.97 MB | Adobe PDF | View/Open Request a copy | |
camedda-education-signed.pdf Restricted Access | 485.93 kB | Adobe PDF | View/Open Request a copy |
This item is licensed under a Creative Commons License