The title alkaloid was synthesized in racemic form from 3, 7-diallyl-2, 4, 6, 8-tetraoxo-3, 7- diazabicyclo [3.3. 1] nonane (7) by a regioselective diallylation reaction followed by double ring-closing olefin metathesis and exhaustive reduction. Tetraoxobispidine 7 was itself prepared in three simple operations from dimethyl malonate. The entire sequence to α- isosparteine was conducted on a multigram scale and proceeded without recourse to ...