Talk:Diels–Alder reaction
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Predicting sterochemistry edit
It is not true for the endo transition state that the substituents on dienophile and 1,4-substituents on diene will always point towards the same side of the newly formed ring...In the picture below, it just happens that the endo transition state will yield substituents on same side of the ring.
can be very unclear to someone who does not realize that Cp is one of the few, if not only dienes with bulky substituents naturally in the inner position. I favor stating the rules which say
"out-endo-cis" (corollary "out-exo-trans")
"in-exo-cis"
where "out" or "in" refer to the position of a diene substituent, "endo" or "exo" refer to the orientation of the dienophile substituent, and "cis" or "trans" refer to the stereochemistry of the two substituents in question.
Thoughts?
Image problems: epimerization edit
The figure titled "Epimerization in DA reaction" could do with some alterations. Firstly structure B loses a methylgroup. Secondly for an easier to understand diagram i believe the hydrogen's on stereocenters should be included in the twistchair conformations — Preceding unsigned comment added by 124.168.1.29 (talk) 05:56, 20 February 2013 (UTC)
Why is the Named Dienes diagram so huge? edit
That can't be right. How do we get it to be a normal size? 128.101.184.163 (talk) 15:24, 16 May 2014 (UTC)
External links modified edit
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Undue emphasis on total synthesis edit
The section on uses seems to be highly focused on listing US-all stars who use this reaction that was discovered before almost all of them were born. The section is an excellent overview or perspective on selected applications of D-A reaction in total synthesis. But..., we probably want readers to learn about where the reaction is used in the real world vs its applications to total syntheses, few of which are practiced. One idea would be to create a separate article or section on historical development of D-A reaction. That is what I did today. But other editors might have better ideas.--Smokefoot (talk) 18:17, 27 December 2017 (UTC)
- Also many reaction schemes show much more than the D-A reaction. So I cropped one to remove the tangential info. If and when I become more skilled with cropping, I may do others. --Smokefoot (talk) 14:58, 23 September 2022 (UTC)
- Perhaps this review could provide some better examples doi:10.1002/anie.201201636 e.g. Buprenorphine. There's likely some simple industrial process which escape academic interest but which operate at significant quantities, 4-vinylcyclohexene might qualify. Captan and Captafol look likely to involve DA chemistry --Project Osprey (talk) 22:52, 24 September 2022 (UTC)
- Industrial uses of D–A? PMID:23447554 is a 2013 review, and Derek Lowe has an article[1]. DMacks (talk) 03:26, 25 September 2022 (UTC)
- Perhaps this review could provide some better examples doi:10.1002/anie.201201636 e.g. Buprenorphine. There's likely some simple industrial process which escape academic interest but which operate at significant quantities, 4-vinylcyclohexene might qualify. Captan and Captafol look likely to involve DA chemistry --Project Osprey (talk) 22:52, 24 September 2022 (UTC)