Abstract
Some new aryloxy[4]ferrocenophanedienes are described, which have been obtained by reaction of 1,1′-di(1-propynyl)ferrocene and respective phenols. These include one case of a twofold reaction of this type. The possibility of using the products as substrates in Diels-Alder cycloadditions was evaluated with the result that only the most reactive dienophile, 4-phenyl-1,2,4-triazoline-3,5-dione, underwent this reaction. The cycloadduct has an unprecedented structure in that the ferrocene moiety 1,4-diaxially caps a boat conformer of a cyclohexane moiety.
| Original language | English |
|---|---|
| Article number | st-2015-b0066-l |
| Pages (from-to) | 1450-1454 |
| Number of pages | 5 |
| Journal | Synlett |
| Volume | 26 |
| Issue number | 11 |
| DOIs | |
| Publication status | Published - 16 Apr 2015 |
Keywords
- 1 1′-dialkynylferrocene
- boat conformation
- Diels-Alder cycloaddition
- ferrocenophane
ASJC Scopus subject areas
- Organic Chemistry
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