Abstract
Some acylated o-amino-7-hydroxycoumarins have been obtained which may be used as intermediates in the preparation of fluorogenic substrates for certain enzymes.
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G. A. Grabowski, T. Dinur, S. Gatt, and R. J. Desnick, Clin. Chim. Acta, 124, 123 (1982).
A. E. Gal, R. O. Brady, P. G. Pentchev, S. Furbish, K. Sudzuki, H. Tanaka, and E. L. Schneider, Clin. Chim. Acta, 77, 53 (1977).
A. E. Gal, P. G. Pentchev, and F. J. Fash, Proc. Soc. Exp. Biol. Med., 153, 363 (1976).
G. T. N. Bresley and A. D. Brain, Clin. Chim. Acta, 88, 226 (1978).
N. M. Shah and R. H. Mehta, J. Indian Chem. Soc., 31, 784 (1954).
Yu. V. Guk, M. A. Ilyushin, E. L. Golod, and B. V. Gidaspov, Usp. Khimii, 52, 498 (1983).
K. D. Kaufman, W. E. Russey, and L. R. Worden, J. Org. Chem., 27, 875 (1962).
W. R. Sherman and E. F. Stainfield, Biochem. J., 102, 905 (1967).
R. H. Mehta and S. Sethna, J. Indian Chem. Soc., 41, 122 (1964).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 906–909, July, 1985.
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Kozlova, I.K. Synthesis of o-acylamino-4-methyl-7-hydroxycoumarins (4-methylumbelliferones). Chem Heterocycl Compd 21, 750–753 (1985). https://doi.org/10.1007/BF00519138
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DOI: https://doi.org/10.1007/BF00519138