Abstract
A preparative method was worked out for the synthesis of 3,4,6-triaryl-2-pyrones by 1,3-dipolar cycloaddition of selenium arylacylmethylides to diphenylcyclopropenone.
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N. N. Magdesieva, R. A. Kyandzhetsian, and V. A. Danilenko, Khim. Geterotsikl. Soedin., No. 11, 1447 (1973).
R. Breslow, T. Eicher, A. Krebs, and R. Peterson, J. Am. Chem. Soc., 87, 1320 (1965).
N. N. Magdesieva, Le Nguyen Ngi, and N. M. Koloskova, Zh. Org. Khim., 13, No. 5, 110 (1977).
C. Broquet and W. Simalty, Tetrahedron Lett., No. 10, 933 (1972).
N. N. Magdesieva, T. A. Balashova, and G. M. Dem'yanova, Khim. Geterotsikl. Soedin., No. 5, 626 (1972).
N. O. Saldabol and S. A. Giller, Izv. Akad. Nauk Latv. SSR, No. 1, 91 (1958).
T. Eicher and E. Angerer, Ann., 746, 120 (1971).
Y. Hayasi and H. Nozaki, Tetrahedron, 27, 3085 (1971).
T. Eicher, E. Angerer, and A. -M. Hansen, Ann., 746, 102 (1971).
P. Metzner and I. Vialla, Bull. Soc. China. France, No. 10, 3739 (1970).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1475–1478, November, 1977.
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Magdesieva, N.N., Koloskova, N.M. & Le Ngi, N. Synthesis of 3, 4, 6-triaryl-2-pyrones. Chem Heterocycl Compd 13, 1177–1180 (1977). https://doi.org/10.1007/BF00475937
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DOI: https://doi.org/10.1007/BF00475937