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Substituent effect of 4-and 5-substituted 2-aryl-methylideneindane-1,3-diones on formation of 5-oxo-1H-4,5-dihydroindeno[1,2-b]pyridines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The ratio of dihydroindenopyridine regioisomers formed from ethyl β-amino-crotonate and 4-or 5-monosubstituted 2-arylideneindane-1,3-dione depends on the total electronic and steric effects of the indanedione substituents.

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References

  1. V. K. Lūsis, D. Kh. Mutseniece, G. Ya. Dubur, [Chem. Heterocycl. Comp., 22, 1104 (1986)].

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Authors and Affiliations

  1. Latvian Institute of Organic Synthesis, Riga, LV-1006, Latvia

    D. Muceniece, J. Popelis & V. Lūsis

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  1. D. Muceniece
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  2. J. Popelis
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  3. V. Lūsis
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Correspondence to V. Lūsis.

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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 42–52, January, 2007.

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Muceniece, D., Popelis, J. & Lūsis, V. Substituent effect of 4-and 5-substituted 2-aryl-methylideneindane-1,3-diones on formation of 5-oxo-1H-4,5-dihydroindeno[1,2-b]pyridines. Chem Heterocycl Comp 44, 35–42 (2008). https://doi.org/10.1007/s10593-008-0014-8

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  • DOI: https://doi.org/10.1007/s10593-008-0014-8

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