Triallyldiindium trihalides and allylindate(1-)s reacted with N-benzylideneamines regioselectively at the C-3 carbon on the allyl group to give high yields of homoallylic secondary amines. Primary amines were obtained by the action of an excess of allylic indates on aromatic nitriles.
三烯丙基二
茚三卤化物和烯丙基
吲哚(1-)酸盐与 N-亚
苄胺在烯丙基上的 C-3 碳处发生了选择性反应,生成了高产率的均烯丙基仲胺。通过过量的烯丙基
吲哚酸盐与芳香族腈的作用,可以得到
伯胺。