Abstract
Methods of synthesis of dienic δ-alkoxy-α, α-dicarbonyl-substituted compounds were experimentally examined. The structure of the synthesized compounds was studied by1H and13C-NMR methods. It was shown that the δ-alkoxy diesters are present in equilibrium with 2H-pyrans, while δ-alkoxy-γ-methyl diesters and 2-(3′-alkoxypropen-2′-ylindene)indanediones exist in an open form and do not undergo cyclization into 2H-pyrans.
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Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 11, pp. 2561–2565, November, 1990.
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Krasnaya, Z.A., Stytsenko, T.S. & Bogdanov, V.S. Synthesis of δ-alkoxy-α, α-dicarbonyl-substituted dienes and study of their valence isomerization. Russ Chem Bull 39, 2316–2321 (1990). https://doi.org/10.1007/BF00958845
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DOI: https://doi.org/10.1007/BF00958845