Talk:Stereochemistry of ketonization of enols and enolates

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The text says One is the treatment of an α-bromoketone with dilute HI in acetone but the image that goes with it shows MeLi V8rik (talk) 21:27, 29 May 2010 (UTC)[reply]

Two reaction conditions had been switched in error and I've fixed the error. Please note detail I've put on the Talk Page of V8rik with thanks to him.

Howard E. Zimmerman 20:24, 30 May 2010 (UTC) —Preceding unsigned comment added by Hezimmerman (talk • contribs)

Thus, a myriad of organic reactions owe their stereochemical control to this phenomenon A partial list is included without extensive detail. Hez (talk) 17:39, 4 November 2011 (UTC)[reply]

Should be rated as "High Importance" — Preceding unsigned comment added by 128.104.69.138 (talk) 15:33, 5 December 2011 (UTC)[reply]

The article was largely written by the late H.E. Zimmerman. He was pretty self-absorbed and wrote a lot about his own work.--Smokefoot (talk) 21:14, 8 September 2020 (UTC)[reply]