Abstract
The reaction of 5-oxotetrahydro-4H-thiochromenes with Grignard reagents has been studied and it has been shown that the reagent adds to the 1,2-position of the conjugated system in the cyclic ketones, The structure of the products depends on that of the starting cyclic ketone.
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References
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Additional information
N. G. Chernyshevskii State University, Saratov 410026. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 613–615, May, 1994. Original article submitted April 22, 1994.
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Markova, L.I., Kharchenko, V.G. Specific reactions of 5-oxotetrahydro-4H-thiochromenes with Grignard reagents. Chem Heterocycl Compd 30, 537–539 (1994). https://doi.org/10.1007/BF01169828
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DOI: https://doi.org/10.1007/BF01169828