Sodium difluoromethanesulfinate—A difluoromethylating agent toward protonated heterocyclic bases
- Авторы: Lytkina M.A.1,2, Eliseenkov E.V.2, Boyarskii V.P.2, Petrov A.A.2
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Учреждения:
- St. Petersburg State Institute of Technology
- St. Petersburg State University
- Выпуск: Том 53, № 4 (2017)
- Страницы: 539-546
- Раздел: Review
- URL: https://journals.rcsi.science/1070-4280/article/view/216050
- DOI: https://doi.org/10.1134/S1070428017040066
- ID: 216050
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Аннотация
Free radical difluoromethylation of protonated heteroaromatic bases was accomplished using sodium difluoromethanesulfinate in combination with tert-butyl hydroperoxide in a two-phase system (methylene chloride–water) at room temperature. The difluoromethylation products of methyl pyridine-4-carboxylate, pyridine-4-carbonitrile, and 2-amino-1,3,4-thiadiazole were isolated on a preparative scale.
Об авторах
M. Lytkina
St. Petersburg State Institute of Technology; St. Petersburg State University
Email: aap1947@yandex.ru
Россия, Moskovskii pr. 26, St. Petersburg, 190005; Universitetskaya nab. 7/9, St. Petersburg, 190005
E. Eliseenkov
St. Petersburg State University
Email: aap1947@yandex.ru
Россия, Universitetskaya nab. 7/9, St. Petersburg, 190005
V. Boyarskii
St. Petersburg State University
Email: aap1947@yandex.ru
Россия, Universitetskaya nab. 7/9, St. Petersburg, 190005
A. Petrov
St. Petersburg State University
Автор, ответственный за переписку.
Email: aap1947@yandex.ru
Россия, Universitetskaya nab. 7/9, St. Petersburg, 190005
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