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Cover Feature: Total Synthesis, Stereochemical Assignment, and Divergent Enantioselective Enzymatic Recognition of Larreatricin (Chem. Eur. J. 59/2018)
Chemistry - A European Journal ( IF 3.9 ) Pub Date : 2018-10-18 , DOI: 10.1002/chem.201805128
Harry J. Martin 1 , Ioannis Kampatsikas 2 , Rik Oost 1 , Matthias Pretzler 2 , Emir Al-Sayed 2 , Alexander Roller 3 , Gerald Giester 4 , Annette Rompel 2 , Nuno Maulide 1
Affiliation  

Mirror, mirror on the wall, who is the fairest one of all? Larreatricin is a naturally occurring lignan with a long history of use in traditional medicine. However, its absolute configuration remains unknown and its biological activity is poorly understood. An efficient total synthesis allowing for the unambiguous assignment of the configuration of its enantiomers is presented. Polyphenol oxidases show high and remarkably divergent enantioselective recognition of this secondary metabolite. More information can be found in the Communication by H. J. Martin, A. Rompel, N. Maulide et al. on page 15756.
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中文翻译:

封面人物:Larreatricin的总合成,立体化学分配和不同的对映选择性酶识别(Chem.Eur.J.59 / 2018)

镜子,墙上的镜子,谁是最美的?Larreatricin是天然存在的木脂素,在传统医学中具有悠久的使用历史。然而,其绝对构型仍然未知,并且其生物学活性还知之甚少。提出了一种有效的全合成方法,可以明确分配其对映异构体的构型。多酚氧化酶对该次级代谢产物显示出很高且显着不同的对映选择性识别。可以在H. J. Martin,A。Rompel,N。Maulide等人的《通讯》中找到更多信息。在第15756页。
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更新日期:2018-10-18
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