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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Aldol condensation reactions of tricarbonyliron complexes. Easy access to diastereomerically pure 1,2,3-trisubstituted 1,3-diols from #alpha#-substituted dienone complexes
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Aldol condensation reactions of tricarbonyliron complexes. Easy access to diastereomerically pure 1,2,3-trisubstituted 1,3-diols from #alpha#-substituted dienone complexes

机译:三羰基铁配合物的羟醛缩合反应。容易从#alpha#取代的二烯酮络合物中获得非对映体纯的1,2,3-三取代的1,3-二醇

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摘要

Tricarbonyliron complexes of #alpha#-substituted dienones are well suited starting compounds for the synthesis of diastereomerically pure 1,2,3-trisubstituted 1,3-diols of known configuration, among them 1,2,3-triols. This is achieved by aldol condensation with an aldehyde, a reaction which gives one distinctly major isolated ketol, under Mukayiama conditions, followed by totally stereoselective reduction.
机译:α-α-取代的二烯酮的三羰基铁配合物非常适合用于合成非对映体纯的已知构型的1,2,3-三取代的1,3-二醇,其中包括1,2,3-三醇。这是通过使醛醇缩醛与醛缩合而实现的,该反应在Mukayiama条件下产生了一种明显主要的分离的酮醇,然后进行完全立体选择性还原。

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