A novel azulene synthesis from the Ramirez ylide involving two different modes of its reaction with activated alkynes

Chem Commun (Camb). 2004 Mar 21:(6):684-5. doi: 10.1039/b316759c. Epub 2004 Feb 11.

Abstract

The Ramirez ylide undergoes electrophilic substitution with acetylenedicarboxylates to form Z and E adducts. The latter can react by cycloaddition with another equivalent of the alkyne to provide a new route to novel tetra-substituted azulenes, which show interesting bond localisation and crystal packing effects.