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Direct, enantioselective aldol coupling of aldehydes using chiral organic catalysts

机译:使用手性有机催化剂对醛进行直接,对映选择性的醛醇缩合

摘要

Nonmetallic, chiral organic catalysts are used to catalyze an enantioselective aldol coupling reaction between aldehyde substrates. The reaction may be carried out with a single enolizable aldehyde, resulting in dimerization to give a β-hydroxy aldehyde, or trimerization to give a dihydroxy tetrahydropyran. The reaction may also conducted with an enolizable aldehyde and a second aldehyde, which may or may not be enolizable, so that the coupling is a cross-aldol reaction in which the α-carbon of the enolizable aldehyde adds to the carbonyl carbon of the second aldehyde in an enantioselective fashion. Reaction systems composed of at least one enolizable aldehyde, an optional additional aldehyde, and the nonmetallic chiral organic catalyst are also provided, as are methods of implementing the enantioselective aldol reaction in the synthesis of sugars.
机译:非金属手性有机催化剂用于催化醛底物之间的对映选择性羟醛偶联反应。该反应可以用单个可烯化的醛进行,导致二聚反应得到β-​​羟基醛,或三聚反应得到二羟基四氢吡喃。该反应还可以与可烯化的醛和可以或不可以烯化的第二种醛进行,使得偶联是一种交叉-羟醛反应,其中可烯化的醛的α-碳加到第二种的羰基碳上。醛以对映选择性的方式。还提供了由至少一种可烯化醛,任选的另外的醛和非金属手性有机催化剂组成的反应体系,以及在糖的合成中实施对映选择性醛醇缩合反应的方法。

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