Some Features of Phosphorylation of 4-Substituted Thiosemicarbazides with Chloroethynylphosphonates
- Autores: Egorov D.1, Chernov I.1, Popchuk M.1, Polukeev V.2, Dogadina A.1
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Afiliações:
- St. Petersburg State Institute of Technology (Technical University)
- Institute of Experimental Medicine
- Edição: Volume 89, Nº 10 (2019)
- Páginas: 2036-2043
- Seção: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/223111
- DOI: https://doi.org/10.1134/S1070363219100086
- ID: 223111
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Resumo
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.
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Sobre autores
D. Egorov
St. Petersburg State Institute of Technology (Technical University)
Email: dog_alla@mail.ru
Rússia, Moskovskii pr. 26, St. Petersburg, 190013
I. Chernov
St. Petersburg State Institute of Technology (Technical University)
Email: dog_alla@mail.ru
Rússia, Moskovskii pr. 26, St. Petersburg, 190013
M. Popchuk
St. Petersburg State Institute of Technology (Technical University)
Email: dog_alla@mail.ru
Rússia, Moskovskii pr. 26, St. Petersburg, 190013
V. Polukeev
Institute of Experimental Medicine
Email: dog_alla@mail.ru
Rússia, St. Petersburg
A. Dogadina
St. Petersburg State Institute of Technology (Technical University)
Autor responsável pela correspondência
Email: dog_alla@mail.ru
Rússia, Moskovskii pr. 26, St. Petersburg, 190013