![](/images/gifchars/alpha.gif)
-Imino anions are generated under neutral reaction conditions via a Pd-mediated decarboxylation of allyl diphenylglycinate imines withconcomitant formation of a
![](/images/gifchars/pi.gif)
-allylpalladium species. The resulting delocalized anion can attack the
![](/images/gifchars/pi.gif)
-allyl-Pd(II) species or be intercepted byaldehydes to afford homoallylic amines or protected 1,2-amino alcohols, respectively.