Cu(I)-assisted carbon---carbon bond forming reactions of γ,γ-dialkoxyallylic zirconium species: a new versatile homoenolate equivalent of propionate |
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Authors: | Azusa Sato Hisanaka Ito Yusuke Yamaguchi Takeo Taguchi |
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Institution: | Tokyo University of Pharmacy & Life Science, 1432-1 Horinouchi, Hachioji, Tokyo 192-0392, Japan |
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Abstract: | In the presence of CuCN, reaction of γ,γ-dialkoxyallylic zirconium species 1 with acyl chloride or allylic phosphates proceeded at the -position of 1 to give alkanoates 3 after aqueous work-up. The ketene dialkylacetal moiety in the coupling products 2 can be used for further bond forming reaction with electrophiles such as nitrosobenzene, nitrostyrene or trichloroacetylisocyanate. |
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Keywords: | γ γ-dialkoxyallylic zirconium allyl cuprate homoenolate ketene acetal |
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