Abstract

The three-component reaction of triphenylphosphine, dialkyl acetylenedicarboxylate, and 2-arylideneindane-1,3-dione in dry DME at 0 °C to room temperature resulted in functionalized 4-(triphenyl-λ<sup>5</sup>-phosphanylidene)-1′,3′-dihydrospiro[cyclopentane-1,2′-inden]-2-enes in 65–87% yields. An unusual feature of the reaction is the retention of the triphenylphosphanylidene group in the spiro product.

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