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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 >Proline-catalyzed asymmetric aldol reactions of tetrahydro-4H-thiopyran-4-one with aldehydes
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Proline-catalyzed asymmetric aldol reactions of tetrahydro-4H-thiopyran-4-one with aldehydes

机译:脯氨酸催化四氢-4H-硫代吡喃-4-酮与醛的不对称醛醇缩合反应

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摘要

Proline-catalyzed enantioselective direct intermolecular aldol reactions of tetrahydro-4//-thiopyran-4-one with various aldehydes give anti adducts with high diastereo- and enantioselectivities in moderate to excellent yields.With the aromatic aldehydes best results were obtained in wet DMF whereas dry DMSO generally was superior with the aliphatic aldehydes.Desulfurization of the adducts with Raney Ni provides products equivalent to aldols from 3-pentanone with potential applications in polypropionate synthesis.
机译:脯氨酸催化的四氢-4 //-硫代吡喃-4-酮与各种醛的对映选择性直接分子间羟醛缩合反应可制得高非对映体和对映体选择性的反加合物,收率中等至极好。在湿DMF中,芳族醛的最佳结果干燥的DMSO通常优于脂族醛。用阮内镍(Raney Ni)对加合物进行脱硫可提供与3-戊酮醛醇缩醛相当的产物,并可能在聚丙烯酸酯合成中应用。

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