The photocycloadditions of 2-(dialkylamino)propenenitriles to 1-acetylnaphthalene in d6 benzene as solvent proceed with high directional selectivity by fast and photoreversible formation of [2+2]-cycloadducts (tetrahydrocyclobuta[a]naphthalenes) followed by a slower and photoirreversible formation of [4+2]-cycloadducts (1,4-dihydro-1,4-ethanonaphthalenes). With increasing duration of irradiation the product pattern is shifted towards a mixture of diastereomeric [4+2]-adducts in which the isomer with endo-orientation of the dialkylamino group in the ethano bridge is predominating. The endo-[4+2]-adduct of 2-(dipropylamino)-propenenitrile to 1-acetylnaphthalene was isolated in pure form, and its configuration was unambiguously corroborated by a single crystal X-ray structure analysis. Upon thermal activation it is converted in a small fraction via an intermediate biradical to the thermodyna-mically more stable exo-epimer before it is decomposed to the educts. Methyl 1-naphthoate reacts in the same way as 1-acetylnaphthalene but less efficiently.
| Identifer | oai:union.ndltd.org:DUETT/oai:DUETT:duett-02162005-095955 |
| Date | 16 February 2005 |
| Creators | Zerwes, Ludger |
| Contributors | Prof. Dr. D. Döpp, Prof. Dr. W. Gärtner |
| Publisher | Gerhard-Mercator-Universitaet Duisburg |
| Source Sets | Dissertations and other Documents of the Gerhard-Mercator-University Duisburg |
| Language | German |
| Detected Language | English |
| Type | text |
| Format | application/octet-stream, application/pdf, text/html |
| Source | http://www.ub.uni-duisburg.de/ETD-db/theses/available/duett-02162005-095955/ |
| Rights | unrestricted, I hereby certify that, if appropriate, I have obtained and attached hereto a written permission statement from the owner(s) of each third party copyrighted matter to be included in my thesis, dissertation, or project report, allowing distribution as specified below. I certify that the version I submitted is the same as that approved by my advisory committee. Hiermit erteile ich der Universitaet Duisburg das nicht-ausschliessliche Recht unter den unten angegebenen Bedingungen, meine Dissertation, Staatsexamens- oder Diplomarbeit, meinen Forschungs- oder Projektbericht zu veroeffentlichen und zu archivieren. Ich behalte das Urheberrecht und das Recht das Dokument zu veroeffentlichen und in anderen Arbeiten weiterzuverwenden. |
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