Abstract
Reactions of primary and secondary alcohols with N'-[2-oxo-5-R-furan-3(2H)-ylidene]acylhydrazides resulted in the furan ring decylization to form 2-[2-(arylcarbonyl)hydrazinylidene]-4-alkyl esters of R-4-oxobutanoic acids.
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REFERENCES
Kirikov, A.Yu., Igidov, N.M., Goldstein, A.G., Kotegov, V.P., and Makhmudov, R.R., Nauchnye vedomosti BelGU, Ser. Meditsina. Farmatsiya, 2012, vol. 19, no. 16, p. 135.
Rubtsov, A.E. and Zalesov, V.V., Russ. J. Org. Chem., 2007, vol. 43, no. 5, p. 735. https://doi.org/10.1134/S1070428007050156
Shipilovskikh, S.A. and Rubtsov, A.E., Russ. Chem. Bull., 2014, vol. 63, no. 9, p. 2205. https://doi.org/10.1007/S11172-014-0722-4
Pulina, N.A., Zalesov, V.V., Bystritskaya, O.A., Rubtsov, A.E., and Kutkovaya, N.V., Pharm. Chem. J., 2009, vol. 43, no. 8, p. 444. https://doi.org/10.1007/S11094-009-0334-8
Zalesov, V.V. and Rubtsov, A.E., Chem. Heterocycl. Compd., 2004, vol. 40, no. 2, p. 133. https://doi.org/10.1023/B:COHC.0000027884.75379.14
Kizimova, I.A., Igidov, N.M., Chaschina, S.V., Chernov, I.N., and Rubtsov, A.E., Russ. J. Org. Chem., 2019, vol. 55, no. 11, p. 1704. https://doi.org/10.1134/S1070428019110101
Igidov, N.M., Kiselev, M.A., and Rubtsov, A.E., Russ. J. Org. Chem., 2016, vol. 52, no. 4, p. 526. https://doi.org/10.1134/S1070428016040084
Kiselev, M.A., Igidov, N.M., Chernov, I.N., Toksarova, Y.S., and Rubtsov, A. E., Russ. J. Org. Chem., 2017, vol. 53, no. 6, p. 920. https://doi.org/10.1134/S1070428017060173
Kizimova, I.A., Igidov, N.M., Dmitriev, M.V., Chashchina, S.V., Makhmudov, R.R., and Siutkina, A.I., Russ. J. Gen. Chem., 2019, vol. 89, no. 12, p. 2345. https://doi.org/10.1134/S107036321912003X
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Kizimova, I.A., Igidov, N.M., Kiselev, M.A. et al. Reactions of N'-[2-Oxo-5-R-furan-3(2H)-ylidene]acylhydrazides with Primary and Secondary Alcohols. Russ J Gen Chem 90, 815–821 (2020). https://doi.org/10.1134/S1070363220050096
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DOI: https://doi.org/10.1134/S1070363220050096