Abstract
5-Arylfuran-2,3-diones reacted with heterocyclic enamines of the 2-azaspiro[4.5]deca-1,6,9-trien-8-one series to give products of β-CH-acylation of the enamino fragment. The structure of (2Z,5Z)-3-hydroxy-5-(6,9-dimethoxy-3,3-dimethyl-8-oxo-2-azaspiro[4.5]deca-6,9-dien-1-ylidene)-1-phenylpent-2-ene-1,4-dione was proved by X ray analysis.
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Original Russian Text © V.V. Konovalova, Yu.S. Rozhkova, Yu.V. Shklyaev, P.A. Slepukhin, A.N. Maslivets, 2014, published in Zhurnal Organicheskoi Khimii, 2014, Vol. 50, No. 12, pp. 1798–1801.
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Konovalova, V.V., Rozhkova, Y.S., Shklyaev, Y.V. et al. Acylation of the enamino tautomer of 2-azaspiro[4.5]deca-1,6,9-trien-8-ones with 5-arylfuran-2,3-diones. Crystal and molecular structure of (2Z,5Z)-3-Hydroxy-5-(6,9-dimethoxy-3,3-dimethyl-8-oxo-2-azaspiro[4.5]deca-6,9-dien-1-ylidene)-1-phenylpent-2-ene-1,4-dione. Russ J Org Chem 50, 1779–1782 (2014). https://doi.org/10.1134/S1070428014120112
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DOI: https://doi.org/10.1134/S1070428014120112