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I added a brief overview of the reaction, showing the reagents and conditions necessary. I also wrote a mechanistic overview of how the reaction proceeds through each transition state. — Preceding unsigned comment added by Mpizzuto15 (talk • contribs) 19:40, 22 December 2017 (UTC)
- Mpizzuto15 - Thanks for your additions. Here are some things to consider improve your contribution, should you choose to edit them yourself.
- Figure edit: Please use "ACS Document 1996" settings on ChemDraw as they provide uniform font and more aesthetically pleasing bond/label ratios. Also remove the large font above the scheme. The caption should be sufficient.
- You show carbonate as the base used for enolization, but describe the use of hydroxide. Is there a range of bases that can be used for the Allan-Robinson Reaction? This may be a good addition to the article.
- Please review your description of the mechanism. Some of the language used is inaccurate based on the scheme that is provided.
- Mpizzuto15 - This is a nice addition and I like how concise you are in your edits. Some things to consider.
As Emily said the 1996 format in chemdraw, a very easy switch just copy and paste it over into the new format. Also I would find it and I'm sure others would find it useful to just highlight one or two examples of how this reaction is actually utilized in research. Finally I see that you dont mention anything about the R-groups. Do they both have to be aromatic for the anhydride or just one? What are some limitations with the R-groups. Just a few quick edits that could make the page a little more helpful for people. Great work on this page so far! Mm9656 (talk) 20:24, 27 December 2017 (UTC)