ChemInform Abstract: Pyrrolidine Catalyzed Reactions of Cyclopentadiene with [alpha],[beta]-Unsaturated Carbonyl Compounds: 1,2- versus 1,4-Additions
The pyrrolidine-catalyzed reactions of benzalacetones (I) with cyclopentadiene leads to isolable intermediate Michael adducts (III) and (IV), which are converted into 1,2-dihydropentalenes (V) at longer reaction times.
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Veröffentlicht in: | ChemInform 2015-08, Vol.46 (33) |
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Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | The pyrrolidine-catalyzed reactions of benzalacetones (I) with cyclopentadiene leads to isolable intermediate Michael adducts (III) and (IV), which are converted into 1,2-dihydropentalenes (V) at longer reaction times. |
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ISSN: | 0931-7597 1522-2667 |
DOI: | 10.1002/chin.201533059 |