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FeCl<sub>3</sub> Catalyzed Regioselective <i>C</i>‑Alkylation of Indolylnitroalkenes with Amino Group Substituted Arenes

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NIAID Data Ecosystem2026-03-08 收录
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An efficient FeCl3 catalyzed protocol for the synthesis of amino functionalized indolyl­nitro­alkanes from easily available precursor indolyl­nitroalkenes and substituted amines has been developed. Regioselective C-alkylation in the presence of free amino substituted arenes occurred. The scope of this methodology shows good functional group tolerance, and further, this protocol was used to prepare indolyl­quinoline derivatives.

本研究开发了一种以易得的前体吲哚基硝基烯烃与取代胺为原料,三氯化铁(FeCl₃)催化的高效合成氨基官能化吲哚基硝基烷烃的方法。该反应可在含游离氨基取代芳烃的体系中实现区域选择性C-烷基化。该方法展现出良好的官能团兼容性,且可进一步用于制备吲哚基喹啉衍生物。

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2014-02-21
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