tert-Amino effect in heterocyclic chemistry. Synthesis of hydrogenated spiro derivatives of quinolines / D'yachenko E.V., Glukhareva T.V., Nikolaenko E.F., Tkachev A.V., Morzherin Yu.Yu. // Russian Chemical Bulletin. - 2004. - V. 53, l. 6. - P. 1240-1247.

ISSN:
10665285
Type:
Article
Abstract:
A new method was developed for the one-step synthesis of spiro derivatives of fused quinolines by the reactions of ortho-amino derivatives of benzaldehyde with Meldrum's acid, cyclohexane-1,3-dione, or N,N′-disubstituted barbituric acids.
Author keywords:
cyclization; nitrogen-containing heterocycles; quinoline; spiro derivatives; tert-amino effect
Index keywords:
heterocyclic amine; quinoline derivative; spiro compound; article; chemical structure; cyclization; derivatization; hydrogenation; Knoevenagel condensation; mass spectrometry; physical chemistry; reac
DOI:
10.1023/B:RUCB.0000042280.7172
Смотреть в Scopus:
https://www.scopus.com/inward/record.uri?eid=2-s2.0-4644219604&doi=10.1023%2fB%3aRUCB.0000042280.71728.d0&partnerID=40&md5=585effbd2ec232c8b6dab0ca7bd26bd2
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Link https://www.scopus.com/inward/record.uri?eid=2-s2.0-4644219604&doi=10.1023%2fB%3aRUCB.0000042280.71728.d0&partnerID=40&md5=585effbd2ec232c8b6dab0ca7bd26bd2
Affiliations Urals State Technical University, 19 Ul. Mira, 620002 Ekaterinburg, Russ. Fed., Russian Federation; N. N. Vorozhtsov Novosibirsk I., Siberian Br. Russ. Acad. of Sci., 9 Prosp. Akad. Lavrenteva, 630090 N., Russian Federation
Author Keywords cyclization; nitrogen-containing heterocycles; quinoline; spiro derivatives; tert-amino effect
References Meth-Cohn, O., Suschitzky, H., (1972) Adv. Heterocycl. Chem., 14, p. 211; Pinnow, J., (1895) Ber. Dtsch. Chem. Ges., 28, p. 3039; Grantham, R.K., Meth-Cohn, O., (1969) J. Chem. Soc., C, p. 70; Martin, J., Meth-Cohn, O., Suschitzky, H., (1973) Tetrahedron Lett., 14, p. 4495; Suschitzky, H., Walrond, R.E., Hull, R., (1977) J. Chem. Soc., Perkin Trans. 1, p. 47; Kirschke, R., Möller, A., Schmaltz, E., Kuban, R.J., Schulz, B., (1986) Tetrahedron Lett., 27, p. 4281; Nijhuis, W.H.N., Verboom, W., Harkema, S., Reinhoudt, D.N., (1989) Red. Trav. Chim. Pays-Bas, 108, p. 147; Cheng, Y., Ye, H.-L., Zhan, Y.-H., Meth-Cohn, O., (2001) Synthesis, p. 904; Cheng, Y., Yang, H.-B., Liu, B., Meth-Cohn, O., Watkin, D., Humphries, S., (2002) Synthesis, p. 906; Verboom, W., Reinhoudt, D.N., (1990) Rec. Trav. Chim. Pay-Bas, 109, p. 311; Melh-Cohn, O., Suschiizky, H., (1996) Adv. Heterocycl. Chem., 65, p. 1; Ojea, V., Muinelo, I., Quintela, J.M., (1998) Tetrahedron, 54, p. 927; Glukhareva, T.V., D'yachenko, E.V., Morzherin, Yu.Yu., (2002) Khim. Geterotsikl. Soedin., p. 1610; (2002) Chem. Heterocycl. Compd., 38, p. 1426. , Engl. Transl; Nijhuis, W.H.N., Verboom, W., Abu El-Fadl, A., Van Hummel, G.J., Reinhoudt, D.N., (1989) J. Org. Chem., 54, p. 199; Nijhuis, W.H.N., Verboom, W., Reinhoudt, D.N., (1987) Synthesis, p. 641; Verboom, W., Reinhoudt, D.N., Visser, R., Harkema, S., (1984) J. Org. Chem., 49, p. 269
Correspondence Address Urals State Technical University, 19 Ul. Mira, 620002 Ekaterinburg, Russ. Fed.Russian Federation; email: atkachev@nioch.nsc.ru
Language of Original Document English
Abbreviated Source Title Russ. Chem. Bull.
Source Scopus