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

From WikiMD's WELLNESSPEDIA

Original file (2,150 × 421 pixels, file size: 36 KB, MIME type: image/png)

This file is from Wikimedia Commons and may be used by other projects. The description on its file description page there is shown below.

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.
Date
Source Own work
Author Ben Mills
Permission
(Reusing this file)
Public domain This work has been released into the public domain by its author, Benjah-bmm27. This applies worldwide.

In some countries this may not be legally possible; if so:
Benjah-bmm27 grants anyone the right to use this work for any purpose, without any conditions, unless such conditions are required by law.

Captions

Add a one-line explanation of what this file represents

Items portrayed in this file

depicts

inception

21 October 2010

media type

image/png

data size

36,866 byte

height

421 pixel

width

2,150 pixel

checksum

7fee2fb72bb90fa81633ef5d51e1017c7a65a9a5

determination method or standard: SHA-1

File history

Click on a date/time to view the file as it appeared at that time.

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

The following page uses this file:

Retrieved from "https://wikimd.org/wiki/File:Synthesis-of-1,4-dioxin-1994-2D-skeletal.png"