File:Synthesis-of-1,4-dioxin-1994-2D-skeletal.png
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| Description |
Scheme describing the synthesis of 1,4-dioxin, based on R. Alan Aitken, J. I. G. Cadogan and Ian Gosneya (1994). "Effect of ring strain on the formation and pyrolysis of some Diels–Alder adducts of 2-sulfolene (2,3-dihydrothiophene 1,1-dioxide) and maleic anhydride with 1,3-dienes and products derived therefrom". J. Chem. Soc., Perkin Trans. 1: 927–931. DOI:10.1039/p19940000927.. Structure drawn in ChemBioDraw Ultra 12.0. |
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| Date | |||
| Source | Own work | ||
| Author | Ben Mills | ||
| Permission (Reusing this file) |
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| Date/Time | Thumbnail | Dimensions | User | Comment | |
|---|---|---|---|---|---|
| current | 20:40, 12 January 2011 | | 2,150 × 421 (36 KB) | Benjah-bmm27 | indicated that the alkene is oxidised to the epoxide (Reaxys suggests hydrogen peroxide, formic acid, 64 °C) |
| 20:21, 21 October 2010 |  | 2,100 × 371 (35 KB) | Benjah-bmm27 | {{Information |Description = Scheme describing the synthesis of 1,4-dioxin, based on {{cite journal | doi = 10.1039/p19940000927 | journal = J. Chem. Soc., Perkin Trans. 1 | year = 1994 | pages = 927–931 | first1 = R. A. | la |
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