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首页> 外文期刊>Mini-reviews in organic chemistry >Asymmetric Baylis-Hillman reaction: Use of novel chiral aldehydes as electrophiles, chiral base catalysts and auxilliaries
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Asymmetric Baylis-Hillman reaction: Use of novel chiral aldehydes as electrophiles, chiral base catalysts and auxilliaries

机译:不对称Baylis-Hillman反应:使用新型手性醛作为亲电试剂,手性碱催化剂和助剂

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摘要

The present review highlights Our recent research findings in the field of asymmetric Baylis-Hillman reaction. in particular, it elaborates oil the following efficient aids: 1) utilization of sugar-derived acrylates as chiral auxiliary for diastercoselective Baylis-Hillman reaction; 2) use of novel chiral electrophiles such as sugar-derived aldehydes and chiral 2,3-epoxy aldehydes for the diastereoselective Baylis-Hillman reaction to obtain valuable chiral adducts 3) a novel prolinol derivative promoted enantioselective Baylis-Hillman reaction and intramolecular Baylis-Hillman reaction wherein both the aldehyde and acrylate component Structure of the same molecular framework to afford high de 's. This review also covers the related research work from other groups on asymmetric Baylis-Hillman reaction.
机译:本综述着重介绍了我们在不对称Baylis-Hillman反应领域的最新研究成果。特别是,它为油提供了以下有效的助剂:1)利用糖衍生的丙烯酸酯作为非对映选择性Baylis-Hillman反应的手性助剂; 2)将新的手性亲电试剂(例如糖衍生的醛和手性2,3-环氧醛)用于非对映选择性Baylis-Hillman反应以获得有价值的手性加合物3)新的脯氨醇衍生物促进对映选择性Baylis-Hillman反应和分子内Baylis-Hillman反应其中醛和丙烯酸酯组分都在相同分子框架结构中反应得到高de的反应。这篇综述还涵盖了其他小组有关不对称Baylis-Hillman反应的相关研究工作。

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