首页> 美国卫生研究院文献>Beilstein Journal of Organic Chemistry >Regioselective cobalt(II)-catalyzed 2 + 3 cycloaddition reaction of fluoroalkylated alkynes with 2-formylphenylboronic acids: easy access to 2-fluoroalkylated indenols
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Regioselective cobalt(II)-catalyzed 2 + 3 cycloaddition reaction of fluoroalkylated alkynes with 2-formylphenylboronic acids: easy access to 2-fluoroalkylated indenols

机译:氟代烷基化炔烃与2-甲酰苯基硼酸的催化2 + 3环加成反应:易于获得2-氟代烷基化Indenols

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摘要

[2 + 3] cycloaddition reactions of fluorinated alkynes with 2-formylphenylboronic acids under the influence of Co(acac)2·2H2O in two-component solvents of acetonitrile/2-propanol at reflux temperature for 18 h took place smoothly, affording the corresponding fluoroalkylated indenol derivatives in good yields. This reaction shows excellent regioselectivity, giving 2-fluoroalkylated indenols, together with a very small amount of 3-fluoroalkylated indanones as side products.
机译:氟化炔烃与2-甲酰基苯基硼酸的环加成反应在二氧化碳/ 2-丙醇的两组分溶剂中,在回流温度下进行18小时,顺利进行,得到相应的氟代烷基化的Indenol衍生物具有良好的产率。该反应显示出优异的区域选择性,将2-氟烷基化的Indenols与非常少量的3-氟代烷基化茚满酮作为侧产物。

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