File:Synthesis-of-1,4-dioxin-1994-2D-skeletal.png

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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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Author Ben Mills
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Date/TimeThumbnailDimensionsUserComment
current20:40, 12 January 2011Thumbnail for version as of 20:40, 12 January 20112,150 × 421 (36 KB)Benjah-bmm27indicated that the alkene is oxidised to the epoxide (Reaxys suggests hydrogen peroxide, formic acid, 64 °C)
20:21, 21 October 2010Thumbnail for version as of 20:21, 21 October 20102,100 × 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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