One‐Step Synthesis of the 1‐Azaspiro[5.5]undecane Skeleton Characteristic of Histrionicotoxin Alkaloids from Linear Substrates via Hg(OTf)2‐Catalyzed Cycloisomerization

Histrionicotoxin (HTX) alkaloids isolated from the poison arrow frogs possess a unique structure characterized by a 1‐azaspiro[5.5]undecane skeleton common to the HTX family. The unique molecular architecture of HTXs and the interest as potential target drugs have prompted synthetic chemists to promote the total synthesis so far. However, all of the synthetic strategies to access the 1‐azaspiro[5.5]undecane framework of HTXs take a multistep approach from linear starting materials due to stepwise construction of either six‐membered carbo‐ or azacycle. Herein, we report the direct one‐step construction of the 1‐azaspiro[5.5]undecane skeleton from linear amino ynone substrates bearing an N‐methoxycarbonyl group utilizing our mercuric triflate (Hg(OTf)2)‐catalyzed cycloisomerization reaction. The utility of this novel methodology was demonstrated by the total and formal syntheses of HTX‐235A and HTX‐283A, respectively, from the azaspirocycle. A one‐step synthesis of the 1‐azaspiro[5.5]undecane skeleton in histrionicotoxin alkaloids from a linear substrate was realized utilizing a Hg(OTf)2‐catalyzed cycloisomerization reaction. Histrionicotoxin alkaloids as potential target drugs were successfully synthesized via our developed cyclization.