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Palladium-catalyzed ortho-selective C–H hydroxylation of carboxybenzyl-protected benzylamines
Organic Chemistry Frontiers ( IF 5.4 ) Pub Date : 2020-06-02 , DOI: 10.1039/c9qo01523j
Chenyang Dai 1, 2, 3, 4, 5 , Yi Han 1, 2, 3, 4, 5 , Lingling Liu 1, 2, 3, 4, 5 , Zhi-Bin Huang 1, 2, 3, 4, 5 , Da-Qing Shi 1, 2, 3, 4, 5 , Yingsheng Zhao 1, 2, 3, 4, 5
Affiliation  

A convenient approach to synthesize o-hydroxybenzylamine via Pd-catalyzed hydroxylation of benzylamine with a removable Cbz-amide as the directing group was developed. Various functional groups were well tolerated, leading to various substituted o-hydroxybenzylamines in moderate to good yields.

中文翻译:

钯催化羧基苄基保护的苄胺的邻位CH羟基羟基化

开发了一种方便的方法,该方法通过Pd催化苄基胺与可移动的Cbz-酰胺作为导向基团的羟基化反应来合成羟基苄基胺。各种官能团具有良好的耐受性,从而以中等至良好的产率产生了各种取代的羟基苄胺。
更新日期:2020-06-30
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