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水飞蓟宾 A 和 B 的顺反异构化。

cis-trans Isomerization of silybins A and B.

机构信息

Institute of Microbiology, v.v.i. AS CR, Vídeňská 1083, Prague 4, CZ-14220, Czech Republic.

Department of Biochemistry, Faculty of Science, Charles University in Prague, Hlavova 8, CZ-12840 Prague 2, Czech Republic.

出版信息

Beilstein J Org Chem. 2014 May 8;10:1047-1063. doi: 10.3762/bjoc.10.105. eCollection 2014.

Abstract

Methods were developed and optimized for the preparation of the 2,3-cis- and the 10,11-cis-isomers of silybin by the Lewis acid catalyzed (BF3∙OEt2) isomerization of silybins A (1a) and B (1b) (trans-isomers). The absolute configuration of all optically pure compounds was determined by using NMR and comparing their electronic circular dichroism data with model compounds of known absolute configurations. Mechanisms for cis-trans-isomerization of silybin are proposed and supported by quantum mechanical calculations.

摘要

方法被开发并优化,用于通过路易斯酸催化(BF3·OEt2)异构化水飞蓟宾 A(1a)和 B(1b)(反式异构体)来制备 2,3-顺式和 10,11-顺式异构体的水飞蓟宾。通过使用 NMR 并将其电子圆二色谱数据与具有已知绝对构型的模型化合物进行比较,确定了所有光纯化合物的绝对构型。提出了水飞蓟宾顺反异构化的机制,并通过量子力学计算得到支持。

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