Email this article Some Features of Phosphorylation of 4-Substituted Thiosemicarbazides with Chloroethynylphosphonates
- Authors: Egorov D.M.1, Chernov I.S.1, Popchuk M.V.1, Polukeev V.A.2, Dogadina A.V.1
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Affiliations:
- St. Petersburg State Institute of Technology (Technical University)
- Institute of Experimental Medicine
- Issue: Vol 89, No 10 (2019)
- Pages: 2036-2043
- Section: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/223111
- DOI: https://doi.org/10.1134/S1070363219100086
- ID: 223111
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Abstract
The reactions of chloroethynylphosphonates with 4-substituted thiosemicarbazides leads to the predominant formation of dialkyl esters of 5-substituted (1,3,4-thiadiazol-2-yl)methylphosphonic acids with an admixture (up to 31%) of dialkyl [3-amino-2-(alkylimino)-2,3-dihydro-1,3-thiazol-4-yl)phosphonates as a minor product.
About the authors
D. M. Egorov
St. Petersburg State Institute of Technology (Technical University)
Email: dog_alla@mail.ru
Russian Federation, Moskovskii pr. 26, St. Petersburg, 190013
I. S. Chernov
St. Petersburg State Institute of Technology (Technical University)
Email: dog_alla@mail.ru
Russian Federation, Moskovskii pr. 26, St. Petersburg, 190013
M. V. Popchuk
St. Petersburg State Institute of Technology (Technical University)
Email: dog_alla@mail.ru
Russian Federation, Moskovskii pr. 26, St. Petersburg, 190013
V. A. Polukeev
Institute of Experimental Medicine
Email: dog_alla@mail.ru
Russian Federation, St. Petersburg
A. V. Dogadina
St. Petersburg State Institute of Technology (Technical University)
Author for correspondence.
Email: dog_alla@mail.ru
Russian Federation, Moskovskii pr. 26, St. Petersburg, 190013
