Talk:Allylic rearrangement

Stereochemistry
Is this really correct??? — Preceding unsigned comment added by Slavefortheempire (talk • contribs) 03:07, 22 January 2011 (UTC)

The stereochemistry of the olefin for the allyl shift may not be correct in reference 5 and 6.

--theslave (talk) 03:23, 22 January 2011 (UTC)

The reaction in ref. 5 is allylboration, that is, allylation of aldehyde with allylboronic acid. The explanation in "Electrophilic allyl shifts" is not correct. In this case, allylic alcohol is converted into allylboronic acid in situ by Pd catalyst and diboronic acid. Allylboronic acid reacts with benzaldehyde, which is activated by p-toluenesulfonic acid.

アズレン (talk) 10:10, 27 July 2017 (UTC)

Images for SNi and SNi' mechanisms
Could someone please upload images of the aforementioned mechanisms? Viv73 (talk) 17:48, 3 May 2019 (UTC)