Preparation of dipyrrins from F-BODIPYs by treatment with methanesulfonic acids
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2015
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RSC
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Urieta Mora, J., Lora Maroto, B., Moreno Jiménez, F. et al. «Preparation of Dipyrrins from F-BODIPYs by Treatment with Methanesulfonic Acids». RSC Advances, vol. 5, n.o 84, agosto de 2015, pp. 68676-80. pubs.rsc.org, https://doi.org/10.1039/C5RA14914B.
Abstract
An alternative metal-free soft procedure for the preparation of dipyrrins from F-BODIPYs is reported. The new method makes possible to obtain certain dipyrrin derivatives that were unaccessible from F-BODIPYs to date. To demonstrate the ability of the new procedure, dipyrrins having highly reactive groups, such as chloro, cyano or acetoxyl, have been easily obtained from the corresponding F-BODIPY, which shows the synthetic utility of the reported methodology.
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The article was received on 27 Jul 2015, accepted on 03 Aug 2015 and first published on 03 Aug 2015