通过吲哚与二芳基-1,2-二酮的新型酸催化反应高效合成吲哚并[3,2-a]咔唑。
An efficient synthesis of indolo[3,2-a]carbazoles via the novel acid catalyzed reaction of indoles and diaryl-1,2-diones.
作者信息
Nair Vijay, Nandialath Vidya, Abhilash Keecherikunnel G, Suresh Eringathodi
机构信息
Organic Chemistry Section, National Institute for Interdisciplinary Science and Technology (formerly known as RRL) (CSIR), Trivandrum, 695019, Kerala, India.
出版信息
Org Biomol Chem. 2008 May 21;6(10):1738-42. doi: 10.1039/b803009j. Epub 2008 Apr 8.
DOI:10.1039/b803009j
PMID:18452007
Abstract
A mild and efficient one pot method for the synthesis of indolo[3,2-a]carbazole derivatives by the para-toluenesulfonic acid catalyzed condensation of indole with acyclic 1,2-diones is described. With cyclobutene-1,2-diones the reaction afforded indole substituted carbazole derivatives in good yield.
摘要
描述了一种温和且高效的一锅法，用于通过对甲苯磺酸催化吲哚与无环1,2 - 二酮的缩合反应来合成吲哚并[3,2 - a]咔唑衍生物。对于环丁烯 - 1,2 - 二酮，该反应能以良好的产率得到吲哚取代的咔唑衍生物。
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