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首页> 外文期刊>The Journal of Organic Chemistry >Synthesis of Cyclohexane-Fused Isocoumarins via Cationic Palladium(II)-Catalyzed Cascade Cyclization Reaction of Alkyne-Tethered Carbonyl Compounds Initiated by Intramolecular Oxypalladation of Ester-Substituted Aryl Alkynes
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Synthesis of Cyclohexane-Fused Isocoumarins via Cationic Palladium(II)-Catalyzed Cascade Cyclization Reaction of Alkyne-Tethered Carbonyl Compounds Initiated by Intramolecular Oxypalladation of Ester-Substituted Aryl Alkynes

机译:通过阳离子钯(II)催化的酯键取代的芳基炔烃的分子内氧羰基化引发的炔烃系链的羰基化合物的级联环化反应合成环己烷熔合的香豆素

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摘要

A cationic Pd(II)-catalyzed cascade cyclization reaction of alkyne-tethered carbonyl compounds was developed. This reaction is initiated by intramolecular oxypalladation of alkynes with an ester group followed by 1,2-addition of the formed C-Pd(II) bond to the carbonyl group, providing a highly efficient method for the synthesis of cyclohexane-fused isocoumarins.
机译:开发了阳离子Pd(II)催化的炔烃系羰基化合物的级联环化反应。该反应由具有酯基的炔烃的分子内氧palpalpalation开始,然后将形成的C-Pd(II)键与羰基进行1,2-加成,从而为合成环己烷稠合的异香豆素提供了一种高效方法。

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