American Chemical Society
ol901334c_si_003.pdf (3.02 MB)

Phosphine-Mediated Olefination between Aldehydes and Allenes: An Efficient Synthesis of Trisubstituted 1,3-Dienes with High E-Selectivity

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journal contribution
posted on 2009-08-06, 00:00 authored by Silong Xu, Lili Zhou, San Zeng, Renqin Ma, Zhihong Wang, Zhengjie He
The phosphine-mediated olefination of aldehydes with electron-deficient allenes to afford trisubstituted conjugated dienes in fair to excellent yields with high E-selectivity is described. The reaction represents a new reactivity pattern of allenes with aldehydes and also provides a highly stereoselective synthetic method for preparing conjugated dienes. In the reaction, the phosphine acts as a nucleophilic promoter to generate in situ an active phosphorus ylide which mediates the intermolecular olefination.