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Original Articles

Topochemical Solid State [2+2] Cyclodimerisations of Enones: Theoretical Considerations

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Pages 53-58 | Published online: 22 Sep 2006
 

Abstract

Molecular orbital calculations using the MNDO computer program were used to study the solid state [2+2] cycloaddition of conjugated enones. Benzylidene methyl ketone was used as a model molecule. The reactive species was identified as a triplet excited state. These calculations were used to clarify the mechanism of this reaction, and to interpret cases of apparent breakdown of the topochemical principle.

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