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Chan-Lam交叉偶联反应在含强供电子或吸电子基团的N-杂环卡宾前体合成中的应用。

Application of Chan-Lam cross coupling for the synthesis of N-heterocyclic carbene precursors bearing strong electron donating or withdrawing groups.

作者信息

Huang Liliang, He Chengxiang, Sun Zhihua

机构信息

College of Chemistry and Chemical Engineering, Shanghai University of Engineering Science, 333 Longteng Road, Shanghai 201620, China.

出版信息

Sci Rep. 2015 Jul 23;5:12431. doi: 10.1038/srep12431.

Abstract

Chan-Lam cross coupling allowed efficient synthesis of N,N'-disubstituted ortho-phenylene diamines bearing strong electron donating or withdrawing groups, such as nitro or methoxy groups, with moderate to high yields. These diamines can then be turned into N-heterocyclic carbene precursors after condensation with trimethyl orthoformate. The same strategy can also be utilized for the synthesis of N-monosubstituted aniline derivatives containing a functionalized ortho-aminomethyl group as intermediates for chiral 6-membered ring carbene precursors.

摘要

Chan-Lam交叉偶联反应能够以中等到高的产率高效合成带有强供电子或吸电子基团(如硝基或甲氧基)的N,N'-二取代邻苯二胺。这些二胺在与原甲酸三甲酯缩合后可转化为N-杂环卡宾前体。同样的策略也可用于合成含有官能化邻氨基甲基的N-单取代苯胺衍生物,作为手性六元环卡宾前体的中间体。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8242/5378884/44dec6c18a54/srep12431-f1.jpg

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