首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Synthesis of Non-Conjugated Trienes via In Situ Hydrovinylation/Wittig Olefination of Unsaturated Phosphonium Salts
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Synthesis of Non-Conjugated Trienes via In Situ Hydrovinylation/Wittig Olefination of Unsaturated Phosphonium Salts

机译:不饱和膦盐的原位氢烷基化/ Wittig烯烃的合成非共轭性烯烃

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摘要

A cobalt-catalysed 1,4-hydrovinylation reaction is successfully applied in a sequential three-component transformation of unsaturated phosphonium bromides, 1,3-dienes, and aldehydes leading to non-conjugated products with a 1,4-diene subunit in good to excellent yields. The hydrovinylation provides regioselectively diene structures with one exo double bond whereas the third double bond can be introduced via an in situ Wittig or Horner-Wadsworth-Emmons olefination leading to 1,4,7-trienes suitable for further double bond functionalisations.
机译:成功地应用了钴催化的1,4-肼化反应在不饱和鏻溴化物,1,3-二烯和醛的序贯三组分转化中,导致非共轭产物,其良好的1,4-二烯亚基 优异的产量。 氢苄基化提供具有一个EXO双键的区域选择性二烯结构,而第三双键可以通过原位Wittig或Horner-Wadsworth-Emmons烯烯来引入,其导致1,4,7-三烯,适用于进一步的双键官能化。

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