首页> 外文期刊>Advanced synthesis & catalysis >A Direct C—C Cross-Coupling of Alcohols at the β-Position with Aldehydes under Co-Promotion of Tris(triphenylphosphine)- rhodium Chloride/Boron Trifuoride Etherate
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A Direct C—C Cross-Coupling of Alcohols at the β-Position with Aldehydes under Co-Promotion of Tris(triphenylphosphine)- rhodium Chloride/Boron Trifuoride Etherate

机译:三(三苯基膦)-氯化铑/三氟硼酸硼盐共促进下,β-位置上的醇与醛的直接CC交联

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摘要

The novel tris(triphenylphosphine)rhodi-um chloride/boron trifuoride etherate [RhCl-(PPh3)3/BF3·OEt2] co-promoted the C—C cross-coupling of tertiary alcohols at the β-position with aldehydes. This reaction provides an efficient synthesis of either structurally diverse 1,3-diols or polysubsti-tuted tetrahydropyrans by controlling the substrate structures, and it could be developed to a practical synthetic method for numerous natural products and medicinally important compounds.
机译:新型的三(三苯基膦)氯化铑/三氟硼化硼醚化物[RhCl-(PPh3)3 / BF3·OEt2]共同促进了叔醇在β-位与醛的C-C交叉偶联。通过控制底物结构,该反应可有效合成结构多样的1,3-二醇或多取代的四氢吡喃,可以开发为多种天然产物和重要医学化合物的实用合成方法。

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