A straightforward, environmentally benefcial synthesis of spiro[diindeno[1,2‑b:2′,1′‑e]py ridine‑11,3′‑indoline]‑2′,10,12‑tri ones mediated by a nano‑ordered reusable catalyst
dc.contributor.author | Demchuk, Oleg M. | |
dc.contributor.author | Fathi, Mahsa | |
dc.contributor.author | Naimi-Jamal, M. Reza | |
dc.contributor.author | Dekamin, Mohammad G. | |
dc.contributor.author | Panahi, Leila | |
dc.date.accessioned | 2022-06-23T09:51:23Z | |
dc.date.available | 2022-06-23T09:51:23Z | |
dc.date.issued | 2021 | |
dc.description.abstract | A library of new spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-indoline]-2′,10,12-trione derivatives has been prepared in an efficient, one-pot pseudo four-component method mediated by a reusable heterogeneous nano-ordered mesoporous SO3H functionalized-silica (MCM-41-SO3H) catalyst. Excellent yields, short reaction times, as well as convenient non-chromatographic purification of the products and environmental benefits such as green and metal-free conditions constitute the main advantages of the developed synthetic methodology. The obtained fused indole-indenone dyes would be of interest to pharmaceutical and medicinal chemistry. Furthermore, due to their sensitivity to pH changes, they could be used as novel pH indicators. | pl |
dc.identifier.citation | "Scientifc Reports", 2021, Vol. 11, 4820 | pl |
dc.identifier.doi | 10.1038/s41598-021-84209-6 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12153/3233 | |
dc.language.iso | en | pl |
dc.publisher | Nature Research | pl |
dc.rights | Uznanie autorstwa-Użycie niekomercyjne-Bez utworów zależnych 3.0 Polska | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/pl/ | * |
dc.title | A straightforward, environmentally benefcial synthesis of spiro[diindeno[1,2‑b:2′,1′‑e]py ridine‑11,3′‑indoline]‑2′,10,12‑tri ones mediated by a nano‑ordered reusable catalyst | pl |
dc.type | info:eu-repo/semantics/article | pl |
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