Features of the reaction of 3,4-dihydroxy-6-oxo-2,4-alkadienoic acid esters with acetone and p-toluidine / Mukovoz P.P., Slepukhin P.A., Koz'Minykh V.O., Andreeva V.A., El'Tsov O.S., Ganebnykh I.N., Koz'Minykh E.N. // Russian Journal of General Chemistry. - 2015. - V. 85, l. 12. - P. 2715-2720.

ISSN:

10703632

Type:

Article

Abstract:

Three-component reactions of 3,4-dihydroxy-6-oxo-2,4-alkadienoic acids with acetone and p-toluidine were studied; their specific feature was the formation of the regioisomeric esters of 4-hydroxy-2,2-dimethyl-1-(4-methylphenyl)-5-(2-oxoalkyliden)-2,5-dihydro-1H-pyrrole-3-carboxylic acids and [4-alkanoyl-3-hydroxy-5,5-dimethyl-1-(4-methylphenyl)-1,5-dihydro-2H-pyrrol-2-ylidene]acetic acid. Structure of the synthesized compounds was discussed based on the data of IR and 1H NMR spectroscopy and X-ray diffraction analysis. © 2015 Pleiades Publishing, Ltd.

Author keywords:

2,5-dihydro-1H-pyrrole-3-carboxylic acids esters; 3,4,6-trioxoalkanoic acids esters; azomethines; Schiff bases

Index keywords:

нет данных

DOI:

10.1134/S1070363215120087

Смотреть в Scopus:

https://www.scopus.com/inward/record.uri?eid=2-s2.0-84957551630&doi=10.1134%2fS1070363215120087&partnerID=40&md5=ee75ee9407036c52b1011b3a3c6f15b2

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Поле	Значение
Link	https://www.scopus.com/inward/record.uri?eid=2-s2.0-84957551630&doi=10.1134%2fS1070363215120087&partnerID=40&md5=ee75ee9407036c52b1011b3a3c6f15b2
Affiliations	Institute of Cellular and Intracellular Symbiosis, Ural Branch, Russian Academy of Sciences, ul. Pionerskaya 11, Orenburg, Russian Federation; Perm State Humanitarian-Pedagogical University, Perm, Russian Federation; Yeltsin Ural Federal University, Yekaterinburg, Russian Federation; Postovskii Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Yekaterinburg, Russian Federation; Orenburg State University, Orenburg, Russian Federation
Author Keywords	2,5-dihydro-1H-pyrrole-3-carboxylic acids esters; 3,4,6-trioxoalkanoic acids esters; azomethines; Schiff bases
References	Perevalov, S.G., Burgart, V.Ya., Saloutin, V.I., Chupakhin, O.N., (2001) Russ. Chem. Rev., 70 (11), p. 921. , 1:CAS:528:DC%2BD38XjtVOisr0%3D; Koz'Minykh, V.O., Igidov, N.M., Zykova, S.S., Kolla, V., Shuklina, N.S., (2002) Pharm. Chem. J., 36 (4), p. 188; Yamashkin, S.A., Zhukova, N.V., (2008) Chem. Heterocycl. Compd., 44 (2), p. 115. , 1:CAS:528:DC%2BD1cXpt1Smtrs%3D; Zykova, S.S., Odegova, T.F., Boichuk, S.V., Galembikova, A.R., (2014) Pharm. Chem. J., 48 (11), p. 10; Andreeva, V.A., Mukovoz, P.P., Slepukhin, P.A., Koz'Minykh, V.O., Abstracts of Book (2015) Int. Theoretical and Practical Conf. "perspektivy Razvitiya Nauki i Obrazovaniya", p. 17; Mukovoz, P.P., Dvorskaya, O.N., Koz'Minykh, V.O., (2011) Izv. Vuzov, Ser. Khim. Khim. Tekhnol., 54 (5), p. 96. , 1:CAS:528:DC%2BC3MXovF2rtbs%3D; Bolgova, A.I., Lugovik, K.I., Subbotina, J.O., Slepukhin, P.A., Bakulev, V.A., Belskaya, N.P., (2013) Tetrahedron, 69, p. 7423. , 1:CAS:528:DC%2BC3sXhtVKhtLnL; Giacovazzo, C., Monaco, H.L., Artioli, G., Viterbo, D., Feraris, G., Gilli, G., Zanotti, G., Catti, M., (2002) Fundamentals of Crystallography, , IUCr Oxford; Hesse, M., Meier, H., Zeeh, B., (2008) Spectroscopic Methods in Organic Chemistry, , Thieme Stuttgart; Sheldrick, G.M., (2008) Acta Crystallogr. (A), 64, p. 112. , 1:CAS:528:DC%2BD2sXhsVGhurzO; Dolomanov, O.V., Bourhis, L.J., Gildea, R.J., Howard, J.A.K., Puschmann, H., (2009) J. Appl. Crystallogr. (A), 42, p. 339. , 1:CAS:528:DC%2BD1MXjsFSnsbg%3D; Mukovoz, P.P., Kozminykh, V.O., Tarasova, V.A., (2014) Russ. J. Org. Chem., 50 (11), p. 1687. , 1:CAS:528:DC%2BC2cXitFKmsbrP
Publisher	Maik Nauka Publishing / Springer SBM
CODEN	RJGCE
Language of Original Document	English
Abbreviated Source Title	Russ. J. Gen. Chem.
Source	Scopus