M. Lounasmaa et al., Total synthesis of (+/-)-deethyleburnamonine and vindeburnol (RU 24722) with the corresponding nitriles as starting material, HETEROCYCLE, 51(5), 1999, pp. 1125-1130
Cyclisation occurred during base treatment of cis-nitrile (5). The resultin
g new imine (6) was converted into the therapeutically important deethylebu
rnamonine (4). Total synthesis of vindeburnol (RU 24722) (3), another impor
tant drug, was achieved in one step starting from the trans-nitrile (9).