首页> 外文期刊>Advanced synthesis & catalysis >Access to Functionalized 3,5-Disubstituted 1,2-Dioxolanes under Mild Conditions through Indium(III) Chloride/Trimethylsilyl Chloride or Scandium(III) Triflate Catalysis
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Access to Functionalized 3,5-Disubstituted 1,2-Dioxolanes under Mild Conditions through Indium(III) Chloride/Trimethylsilyl Chloride or Scandium(III) Triflate Catalysis

机译:通过铟(III)氯化物/三甲基甲硅烷基或钪(III)三种催化剂在温和条件下进行官能化的3,5-二取代的1,2-二氧戊烷

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摘要

Herein we report the use of catalytic amount of scandium(III) triflate or indium(III) chloride (with trimethylsilyl chloride) for the functionalization of endoperoxyacetals through Sakurai or Mukaiyama reactions. These catalysts allow milder and more practical conditions than those previously reported with improvements in scope and reproducibility. This method allows a full catalytic sequence from cyclopropanols to produce desired functionalized 1,2-dioxolanes.
机译:在此,我们报告使用催化量的钪(III)三氟甲磺酸盐(III)氯化铟(用三甲基甲硅烷基氯化物)通过Sakurai或Mukaiyama反应进行内甲氧基缩醛的官能化。 这些催化剂允许比以前报告的范围和再现性提高的那些更温和和更实际的条件。 该方法允许来自环丙醇的完全催化序列以产生所需的官能化1,2-二氧戊烷。

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