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首页> 外文期刊>The Journal of Organic Chemistry >Practical Ruthenium-Catalyzed Cyclocarbonylation of Allenyl Alcohols in 2,4,6-Collidine Leading to alpha,beta-Unsaturated Lactones: Concise Stereoselective Synthesis of (+)-Isomintlactone
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Practical Ruthenium-Catalyzed Cyclocarbonylation of Allenyl Alcohols in 2,4,6-Collidine Leading to alpha,beta-Unsaturated Lactones: Concise Stereoselective Synthesis of (+)-Isomintlactone

机译:实用的钌催化的2,4,6-可力丁中的烯丙基醇的环羰基化反应,导致α,β-不饱和内酯:(+)-异内酯的立体立体选择性合成

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摘要

We have found that ruthenium-catalyzed cyclocarbonylation of allenyl alcohols in 2,4,6-collidine under atmospheric pressure of carbon monoxide smoothly proceeds to afford alpha,beta-unsaturated five- and six-membered lactones in moderate to good yields. Furthermore, we have completed a highly stereoselective synthesis of (+)-isomintlactone by the cyclocarbonylation of allenyl alcohol using 2,4,6-collidine.
机译:我们已经发现,在一氧化碳的大气压下,钌催化的2,4,6-可力丁中的烯丙醇的环羰基化顺利进行,从而以中等至良好的收率得到了α,β-不饱和的五元和六元内酯。此外,我们已经完成了通过使用2,4,6-可力丁对烯丙醇进行环羰基化的(+)-异内酯的高度立体选择性合成。

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