Alkylidenecyclopropanone

Chapter 5 by M. Fujita and T. Okuyama examines the ringopening reactions of alkylidenecyclopropanone acetals for solvolytic generation and trapping of alkylideneallyl cations (resonance hybrids of 1-vinyl-substituted vinyl cations). In Chapter 6 by V. P. Reddy et al. stable ion and computational studies of cyclobutylmethyl cations are discussed. In Chapter 7, G. I. Borodkin and V. G. Shubin discuss and... 

Generation of Alkylideneallyl Cations from Alkylidenecyclopropanone Acetals Selectivity of Reaction with Nucleophiles... 

Ring opening reaction of alkylidenecyclopropanone acetals readily proceeds in the presence of Lewis or Bransted acids to produce l-alkylidene-2-oxyallyl cation, which is provided for the reaction with nucleophiles such as chloride, alcohols, siloxyalkenes, and furans. The reaction of this cation with the carbon nucleophiles gives products of [4 + 3] and [3 + 2] cycloaddition as well as those of nucleophilic addition. The modes of addition reactions are controlled by the oxy group of the cation and by the reaction conditions including solvent. 

We have recently developed a novel method for the generation of alkylideneallyl cations from alkylidenecyclopropanone acetals (8, 9). This method provides a nice opportunity to examine the selectivity of reactions of the ambident cation with various nucleophiles including siloxyalkenes (10) and furans (11). The reaction of the cation with the carbon nucleophiles gives [4 + 3] and [3 + 2] cycloaddition products as well as simple nucleophilic addition products. These results are summarized in this chapter. 

Scheme 5. Regioselective ring opening of alkylidenecyclopropanone acetal...

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