Carbonyl-containing spiro-dihydrofurans in reactions with ammonium acetate and hydrazine hydrate |
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Authors: | O V Fedotova M I Skuratova P V Reshetov M A Panov |
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Institution: | (1) Saratov State University, Saratov, 410026, Russia |
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Abstract: | It has been shown that 2-spiro(3-R-6,6-dimethyl-4-oxo-2,3,4,5,6,7-hexahydrobenzofuran)-2′-(5′, 5′-dimethylcyclohexane-1′,3′-diones)
undergo conversions in reactions with ammonium acetate and hydrazine hydrate into substituted dihydropyridin-2-ones and tetrahydro-1,2-diazepin-7-ones
respectively as a result of ring-opening of the spirodimedonyl fragment through the corresponding amides and hydrazides of
δ-keto acids.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1800–1804. December, 2005. |
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Keywords: | dihydropyridone spirodihydrofuran tetrahydrodiazepinone |
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