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Synthesis of carbonyl compounds based on the products of addition of polyhaloalkanes to unsaturated systems. Reactions of 1-aryl-5,5-dichloropenta-2,4-dien-1-ones with ethyl acetoacetate
Authors:S A Woznesensky  A A Dudinov  L I Belen'kii  M I Struchkova  V N Nesterov  M M Krayushkin  Yu T Struchkov
Institution:(1) N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky prosp., 117913 Moscow, Russian Federation;(2) A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813 Moscow, Russian Federation
Abstract:The reactions of 1-aryl-5,5-dichloropenta-2,4-dien-1-ones with ethyl acetoacetate in the presence of EtONa give ethyl 4-aryl-6-(2,2-dichlorovinyl)-4-hydroxy-2-oxocyclohexane-carboxylates. The structures of the reaction products were confirmed by1H and13C NMR spectroscopy and by X-ray diffraction analysis. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 3, pp.
Keywords:ethyl 4-aryl-6-(2  2-dichlorovinyl)-4-hydroxy-2-oxocyclohexanecarboxylates  synthesis  1-aryl-5  5-dichloropenta-2  4-dien-1-ones  ethyl acetoacetate  condensation  cyclization  crystal structure            1H and13C NMR spectra
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