Abstract
The reactions of arylhydrazides of dialkylglycolic acids with chlorides of α-halocarboxylic acids, followed by cyclization, yielded 2-[hydroxy(dialkyl)methyl]-4-aryl-6,6-disubstituted 4,5-dihydro-6H,1,3,4-oxadiazinones-5.
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J. S. Rao and R. Filler, Chem. Commun., 1622 (1970).
J. von Alphen, Rec. Trav. Chim., 48, 163 (1929).
I. S. Berdinskii, Zh. Obshch. Khim., 28, 1263 (1958).
I. S. Berdinskii and L. N. Krovnikova, Khim. Geterotsikl. Soedin., No. 2, 220 (1967).
I. S. Berdinskii, Zh. Obshch. Khim., 34, 762 (1964).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 7, pp. 896–897, July, 1984.
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Glushkov, V.A., Berdinskii, I.S. 2-[Hydroxy(dialkyl)methyl]-4-aryl-6,6-disubstituted 4,5-dihydro-6H-1,3,4-oxadiazinones-5. Chem Heterocycl Compd 20, 726–728 (1984). https://doi.org/10.1007/BF00506958
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DOI: https://doi.org/10.1007/BF00506958