Gold‐Catalyzed Rearrangements: Reaction Pathways Using 1‐Alkenyl‐2‐alkynylcyclopropane Substrates

José Barluenga, Eva Tudela, R. Vicente, Alfredo Ballesteros, Miguel Tomás

Angewandte Chemie International Edition · 2011 · 48 citations · 33 references

DOIFull text

Open access

Concepts

Abstract

New reactivity patterns: Gold(I) catalyzes the conversion of cyclopentenes (1/1′) into cyclohexadienes (2/3). This profound skeleton rearrangement comprises ring expansion and a [1,2]-alkynyl shift, and is thought to be initiated by the cleavage of the bridging CC bond. The proposed allyl–gold cation intermediate is trapped with alcohols to provide bicyclo[3.2.1]octadiene and tricyclo[3.2.1.02,7]octane derivatives.

References

33