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首页> 外文期刊>Angewandte Chemie >Asymmetric Self- and Cross-Aldol Reactions of Glycolaldehyde Catalyzed by D-Fruetose-6-phosphate Aldolase
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Asymmetric Self- and Cross-Aldol Reactions of Glycolaldehyde Catalyzed by D-Fruetose-6-phosphate Aldolase

机译:D-果糖-6-磷酸醛缩酶催化糖醛的不对称自身和交叉醛醇缩合反应

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摘要

Aldol additions are key chemical reactions for the construction of chiral complex polyhydroxylated molecules. Recent developments in direct aldol additions using bio-, organo-, and metal catalysts are promising since these methodologies do not require separate generation of enolate equivalents and thus improve the atom economy of the transformation. Aldehydes have been regarded as highly interesting donors in aldol reactions, because the products formed are themselves aldehydes that can be used in further aldol additions for the construction of complex polyfunctional molecular frameworks.
机译:醛醇的添加是手性复合物多羟基化分子的构建的关键化学反应。使用生物,有机和金属催化剂直接添加羟醛的最新进展是有希望的,因为这些方法不需要单独生成烯醇盐当量,从而提高了转化的原子经济性。醛被认为是醛醇缩合反应中非常有趣的供体,因为形成的产物本身就是醛,可用于进一步的醛醇加成中,以构建复杂的多功能分子骨架。

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