Diastereoselective Gold‐Catalyzed Cycloisomerizations of Ene‐Ynamides

S. Couty, Christophe Meyer, Janine Cossy

Angewandte Chemie International Edition · 2006 · 172 citations · 60 references

Concepts

Abstract

Around they go: 1,6-Ene-ynamides undergo highly diastereoselective gold-catalyzed cycloisomerizations that lead to functionalized cyclobutanones or carbonyl compounds with a 2-azabicyclo[3.1.0]hexane subunit, depending on the substitution pattern (Ts=p-toluenesulfonyl).

References

60