Abstract
An X-ray structural investigation of N-(2-hydrazono-2-hydroxyethyl)-d-pseudoephedrine is performed, and intramolecular heterocyclization of this compound with orthoformic ester is studied. The final reaction product is found to be a compound containing a morpholone ring rather than substituted 1,3,4-oxadiazole.
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Original Russian Text © I.V. Kulakov, O.A. Nurkenov, A.A. Ainabaev, D.M. Turdybekov, K.M. Turdybekov, A.M. Gazaliev, 2007, published in Zhurnal Obshchei Khimii, 2007, Vol. 77, No. 9, pp. 1538–1541.
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Kulakov, I.V., Nurkenov, O.A., Ainabaev, A.A. et al. Steric structure of N-(2-Hydrazono-2-hydroxyethyl)-d-pseudoephedrine and its intramolecular heterocyclization under the action of orthoformic ester. Russ J Gen Chem 77, 1610–1613 (2007). https://doi.org/10.1134/S1070363207090186
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DOI: https://doi.org/10.1134/S1070363207090186