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Synthesis and the absolute configurations of isoflavanone enantiomers

机译:异黄酮对映体的合成及绝对构型

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Isoflavanone has been synthesized from the reduction of isoflavone in nearly quantitative yield. Isoflavone with seven equivalents of ammonium formate in the presence of Pd/C in ethanol under N-2 atmosphere exclusively produced the two-electron reduced product in two hours. It was characterized by various spectroscopic methods, including UV-VIS, EI-MS, H-1-NMR, C-13-NMR and H-1,H-1-COSY. The racemic mixture was separated by Sumi-Chiral column chromatography and the absolute configurations of the enantiomers were characterized by circular dichroism spectroscopy.
机译:异黄烷酮是通过异黄酮的还原以接近定量的产率合成的。在乙醇中,在Pd / C下,在N-2气氛下,异黄酮与7个当量的甲酸铵可在2小时内专门生成两电子还原的产物。它通过各种光谱方法进行了表征,包括UV-VIS,EI-MS,H-1-NMR,C-13-NMR和H-1,H-1-COSY。外消旋混合物通过Sumi-手性柱色谱法分离,对映体的绝对构型通过圆二色谱法表征。

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