Front Cover: Copper‐Promoted N‐Arylation of the Indole Side Chain of Tryptophan Using Triarylbismuthines (Eur. J. Org. Chem. 36/2020),European Journal of Organic Chemistry

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Front Cover: Copper‐Promoted N‐Arylation of the Indole Side Chain of Tryptophan Using Triarylbismuthines (Eur. J. Org. Chem. 36/2020)
European Journal of Organic Chemistry ( IF 2.5 ) Pub Date : 2020-09-03 , DOI: 10.1002/ejoc.202001188
Adrien Le Roch ₁ , Hwai‐Chien Chan ₁ , Alexandre Gagnon ₁

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The Front Cover shows the copper‐promoted N‐arylation of the indole side chain of tryptophan using triarylbismuth reagents. These reagents are represented by a tripodal spaceship where the aryl groups form the legs of the ship and where a crystal of inorganic bismuth is located in the command center of the unit. The purple spheres illustrate the copper(II) catalyst which is converted into copper(I) at the end of the reaction. More information can be found in the Communication by A. Gagnon et al.

中文翻译：

封面：使用三芳基双突变蛋白对色氨酸的吲哚侧链进行铜促进的N-芳基化反应（Eur。J. Org。Chem。36/2020）

前盖显示了使用三芳基铋试剂对色氨酸的吲哚侧链进行铜促进的N-芳基化。这些试剂由三脚架飞船代表，其中的芳基形成了船的腿，无机铋的晶体位于装置的指挥中心。紫色球表示在反应结束时将铜（II）催化剂转化为铜（I）的催化剂。有关更多信息，请参见A. Gagnon等人的来文。

更新日期：2020-09-23

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