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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >RHODIUM-CATALYZED CYCLOISOMERIZATION OF ALLYL PROPARGYL ETHERS:AN EFFICIENT SYNTHESIS OF 3,4-DISUBSTITUTED FURANS
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RHODIUM-CATALYZED CYCLOISOMERIZATION OF ALLYL PROPARGYL ETHERS:AN EFFICIENT SYNTHESIS OF 3,4-DISUBSTITUTED FURANS

机译:铑催化的丙烯丙基丙二醇的环异构化:高效合成3,4-二取代的呋喃

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摘要

Cycloisomerization of allyl propargyl ethers was found to be catalyzed by a cationic rhodium complex to give 3,4-disubstituted furans in one step.Addition of carboxylic acids to the reaction improved the yield of the products.Generation of a rhodium hydride species from a rhodium complex with the carboxylic acids followed by hydrorhodation of the substrate with the rhodium hydride species would be involved in the reaction pathway.
机译:发现烯丙基炔丙基醚的环异构化是通过阳离子铑络合物催化的,一步即可得到3,4-二取代的呋喃,向反应中添加羧酸可提高产物的产率。从铑生成氢化铑物种与羧酸络合,然后将底物与氢化铑物质加氢水解,将参与反应路径。

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