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Yonemitsu-type condensations catalysed by proline and Eu(OTf)3

机译:脯氨酸和Eu(OTf)3催化的米光缩合反应

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摘要

We report a Yonemitsu-type trimolecular condensation of aromatic heterocycles, aldehydes, and active methylene compounds to afford polyfunctionalised heterocycles. The reaction is catalysed by L-proline and Eu(OTf)3, takes place in methanol at room temperature, and in some cases is highly diastereoselective (d.e. >90%). The reaction offers two advantages with respect to the previously reported Ti(IV)-promoted condensation: (1) it adheres to some principles of green chemistry, and (2) it provides access to compounds that cannot be obtained by classical methodology.
机译:我们报告芳杂环,醛和活性亚甲基化合物的米光型三分子缩合,以提供多官能团的杂环。该反应由L-脯氨酸和Eu(OTf)3催化,在室温下于甲醇中进行,在某些情况下具有很高的非对映选择性(d.e.> 90%)。该反应相对于先前报道的Ti(IV)促进的缩合反应具有两个优点:(1)遵守绿色化学的某些原理,(2)提供了经典方法无法获得的化合物。

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