3-Phosphorylated thioazoles
- Авторы: Egorov D.1, Piterskaya Y.1, Erkhitueva E.1,2, Svintsitskaya N.1, Dogadina A.1
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Учреждения:
- St. Petersburg State Institute of Technology
- St. Petersburg State University
- Выпуск: Том 87, № 9 (2017)
- Страницы: 1924-1933
- Раздел: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/221199
- DOI: https://doi.org/10.1134/S1070363217090067
- ID: 221199
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Аннотация
A novel procedure is reported for the synthesis of 3-phosphorylated N,S-heterocyclic systems by regio- and chemoselective reaction of chloroethynylphosphonates with the thio tautomers of various thioazoles. If the initial sulfanyl azole possesses labile protons or basic NR groups, partial or complete loss of chemoselectivity is observed, and the products are the corresponding acyclic 1,2- and 2,2-substituted alkenylphosphonates.
Об авторах
D. Egorov
St. Petersburg State Institute of Technology
Email: dog_alla@mail.ru
Россия, Moskovskii pr. 26, St. Petersburg, 190013
Yu. Piterskaya
St. Petersburg State Institute of Technology
Email: dog_alla@mail.ru
Россия, Moskovskii pr. 26, St. Petersburg, 190013
E. Erkhitueva
St. Petersburg State Institute of Technology; St. Petersburg State University
Email: dog_alla@mail.ru
Россия, Moskovskii pr. 26, St. Petersburg, 190013; Universitetskii pr. 26, St. Petersburg, 198504
N. Svintsitskaya
St. Petersburg State Institute of Technology
Email: dog_alla@mail.ru
Россия, Moskovskii pr. 26, St. Petersburg, 190013
A. Dogadina
St. Petersburg State Institute of Technology
Автор, ответственный за переписку.
Email: dog_alla@mail.ru
Россия, Moskovskii pr. 26, St. Petersburg, 190013