Abstract
A simple method has been developed for obtaining 9-arylidenedeoxyvasicinones by condensing deoxyvasicinone with aromatic aldehydes in the presence of glacial acetic acid. The yields of reaction products amount to 69–95%.
Similar content being viewed by others
References
Kh. M. Shakhidoyatov, Quinazol-4-ones and their Biological Activity [in Russian], Fan, Tashkent (1988), p. 60.
Kh. M. Shakhidoyatov, A. Irisbaev, É. Oripov, and Ch. Sh. Kadyrov, Khim. Prir. Soedin., 557 (1976).
É. O. Oripov, L. M. Yun, Kh. M. Shakhidoyatov, and Ch. Sh. Kadyrov, Khim. Prir. Soedin., 603 (1978).
Kh. M. Shakhidoyatov, É. O. Oripov, A. Irisbaev, and Ch. Sh. Kadyrov, Khim. Prir. Soedin., 825 (1976).
É. O. Oripov, Kh. M. Shakhidoyatov, Ch. Sh. Kadyrov, and N. D. Abdullaev, Khim. Prir. Soedin., 684 (1979).
Kh. M. Shakhidoyatov, M. Ya. Yamankulov, and Ch. Sh. Kadyrov, Khim. Prir. Soedin., 552 (1977).
B. M. Morris, W. E. Hanford, and R. Adams, J. Am. Chem. Soc.,57, 951 (1935).
R.I. Moskalenko and G. I. Savel'eva, Khim. Geterotsikl. Soedin., 348 (1969).
Additional information
Institute of the Chemistry of Plant Substances, Academy of Sciences of the Republic of Uzbekistan, Tashkent, fax (3712) 40 64 75. Translated from Khimiya Prirodnykh Soedinenii, No. 1, pp. 79–81, January–February, 1998.
Rights and permissions
About this article
Cite this article
Shakhidoyatov, K.M., Kaisarov, I.K. Synthesis of 9-arylidene derivatives of deoxyvasicinone. Chem Nat Compd 34, 59–61 (1998). https://doi.org/10.1007/BF02249688
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF02249688