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Studies on enamides Part-21:A novel photochemical synthesis of 9H-indolo [3,2,1-de] phenanthridin-9-one, a benzcanthine analogue
Tetrahedron ( IF 2.1 ) Pub Date : 1989 , DOI: 10.1016/s0040-4020(01)89239-5
Somnath Ghosh , Diptendu Bhusan Datta , Indira Datta , Tapas Kumar Das

The synthesis of 3-aroylcarbazoles [(a-d)] and the unknown 1-aroylcarbazoles [(a-c)] been achieved by the photolysis of 9-aroylcarbazoles [(a-d)] in polar solvent. Irradiation of (a-c) in non-polar solvent afforded regiospecifically (a-c), carbazole () and for the first time, 9H-indolo [3, 2, 1-de] phenanthridin-9-one () from b. The yield of was significantly improved by UV exposure of 9-(2-iodobenzoyl)-carbazole (e) in methanol and iodine, without providing any photomigrated product.

中文翻译:

酰胺类化合物的研究第2部分1:一种新的光化学合成9H-吲哚并[3,2,1-de]菲啶9-9-,一个苯并鸟氨酸类似物

3-芳酰基咔唑[ (ad)]和未知的1-芳酰基咔唑[ (ac)]的合成是通过9-芳酰基咔唑[ (ad)]在极性溶剂中的光解而实现的。在非极性溶剂中照射(ac),可以从区域上特异性地(ac)提供咔唑(),并首次b中获得9H-吲哚并[3,2,1-de]菲啶9-one(1 )。通过将9-(2-碘苯甲酰基)-咔唑(e)在甲醇和碘中进行UV暴露,无需提供任何光迁移的产物,即可显着提高其产率。
更新日期:2017-01-31
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