Front Cover: Arylation of Aniline C(sp3)−H Bonds with Phenols via an In Situ Activation Strategy (Asian J. Org. Chem. 3/2018),Asian Journal of Organic Chemistry

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Front Cover: Arylation of Aniline C(sp3)−H Bonds with Phenols via an In Situ Activation Strategy (Asian J. Org. Chem. 3/2018)
Asian Journal of Organic Chemistry ( IF 2.8 ) Pub Date : 2018-03-02 , DOI: 10.1002/ajoc.201800107
Yong-Yuan Gui ₁ , Zi-Xiao Wang ₁ , Wen-Jun Zhou _{1,

2} , Li-Li Liao ₁ , Lei Song ₁ , Zhu-Bao Yin ₁ , Jing Li ₁ , Da-Gang Yu ₁

Affiliation

It's the Year of the Dog! Phenols are used as general and efficient arylating reagents through in situ activation in the functionalization of aniline C(sp³)−H bonds via visible‐light photoredox/nickel dual catalysis. This protocol features high step efficiency, time economy, environmental impact, broad substrate scope, high yields, good functional‐group tolerance, and low catalyst loading. More information can be found in the Communication by Wen‐Jun Zhou, Da‐Gang Yu et al. on page 537 in Issue 3, 2018 (DOI: 10.1002/ajoc.201700450).

中文翻译：

封面：通过原位活化策略将苯胺C（sp3）-H键与苯酚丙烯酸化（Asian J. Org。Chem。3/2018）

这是狗年！通过在可见光光氧化还原/镍双重催化作用下苯胺C（sp ³）-H键的功能化中原位活化，苯酚被用作一般有效的芳基化试剂。该方案具有步骤效率高，时间经济，环境影响，底物范围广，产率高，官能团耐受性好和催化剂负载低的特点。有关更多信息，请参见周文俊，余大刚等的《通讯》。就在第3期，2018第537页（：10.1002 / ajoc.201700450 DOI）。

更新日期：2018-03-02

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