Abstract
A number of aryldiazinyl acetonitriles were subjected to hydrolysis, methylation, and benzylation reactions. They resulted in the formation of aryldiazinylacetamides, diazinylmethylacetonitriles, and benzyldiazinylacetonitriles, respectively.
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K. Wisterowicz and H. Foks, Khim. Geterotsikl. Soedin., 1346 (2006). [Chem. Heterocycl. Comp., 42, 1168 (2006)].
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Published in Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1534–1540, October, 2006.
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Wisterowicz, K., Foks, H. Syntheses of new 1,2-, 1,3-, and 1,4-diazine derivatives. 2. Hydrolysis and alkylation of diazinylphenylacetonitriles. Chem Heterocycl Compd 42, 1325–1330 (2006). https://doi.org/10.1007/s10593-006-0242-8
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DOI: https://doi.org/10.1007/s10593-006-0242-8