Asymmetric synthesis of (-)-anatoxin-a via an asymmetric cyclization usinga new ligand for Pd-catalyzed alkylations

Palladium-catalyzed asymmetric allylic alkylations have been explored in th e context of medium-sized ring substrates, intramolecular vs intermolecular processes involving attack on a formally meso pi-allyl intermediate in the desymmetrization, and the presence of electron-withdrawing groups on the c ationic pi-allylpalladium intermediate. The synthesis of anatoxin-a, also k nown as the "very fast death factor", raises all of these questions. Ligand s derived from trans-1,2-diaminocyclohexane and 2-diphenylphosphinobenzoic acid effect asymmetric alkylations with an allyl substrate bearing an elect ron-withdrawing group. On the other hand, a new type of ligand wherein the diamine is derivatized with both 2-diphenylphosphinobenzoic acid and 2-pico linic acid was required to effect asymmetric cyclization to form the 9-azab icyclo[4.2. 1]non-2-ene system. A total synthesis of anatoxin-a from 5-hydr oxy-1,8-nonadiene employing a metathesis reaction to form the cycloheptene and a palladium-catalyzed asymmetric cyclization to form the bicyclic ring system is achieved in 15% overall yield.