A trans diacyloxylation of indoles

Qiang Liu; Qing Yong Zhao; Jie Liu; Pan Wu; Hong Yi; Aiwen Lei

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A trans diacyloxylation of indoles

机译：吲哚的反式二酰氧基化

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A trans diacyloxylation of indoles is accomplished by employing PhI(Oac)2 as the oxidant. A broad range of functional groups are well tolerated. Both the electronic properties of the N-protecting groups of indoles and the acidity of the reaction media play important roles in the selectivity of indole acyloxylation reactions.

机译：吲哚的反式二酰氧基化是通过使用PhI（Oac）2作为氧化剂来完成的。广泛的官能团被很好地耐受。吲哚的N-保护基团的电子性质和反应介质的酸性都在吲哚酰氧基化反应的选择性中起重要作用。

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来源
《Chemical Communications》 |2012年第26期|p.3239-3241|共3页
作者
Qiang Liu; Qing Yong Zhao; Jie Liu; Pan Wu; Hong Yi; Aiwen Lei;
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作者单位

College of Chemistry and Molecular Sciences, Wuhan University,Wuhan, 430072, P. R. China;

College of Chemistry and Molecular Sciences, Wuhan University,Wuhan, 430072, P. R. China;

College of Chemistry and Molecular Sciences, Wuhan University,Wuhan, 430072, P. R. China;

College of Chemistry and Molecular Sciences, Wuhan University,Wuhan, 430072, P. R. China;

College of Chemistry and Molecular Sciences, Wuhan University,Wuhan, 430072, P. R. China;

College of Chemistry and Molecular Sciences, Wuhan University,Wuhan, 430072, P. R. China,State Key Laboratory for Oxo Synthesis and Selective Oxidation,Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, 730000, Lanzhou, P. R. China;

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A trans diacyloxylation of indoles

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