Preparation of Diversely Substituted Triarylmethyl Radicals by the Quenching of Tris(2,3,5,6-tetrathiaaryl)methyl Cations with C-, N-, P-, and S-Nucleophiles Научная публикация
| Журнал |
European Journal of Organic Chemistry
ISSN: 1434-193X , E-ISSN: 1099-0690 |
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| Вых. Данные | Год: 2014, Том: 2014, Номер: 2, Страницы: 371-380 Страниц : DOI: 10.1002/ejoc.201301161 | ||||||||
| Ключевые слова | Carbocations; Radicals; Electron transfer; Nucleophilic addition; Reaction mechanisms | ||||||||
| Авторы |
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| Организации |
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Реферат:
C-, N-, P-, and S-nucleophiles reacted with symmetrical tris(2,3,5,6-tetrathiaaryl)methyl cations, generated from the corresponding triarylmethanols by strong acids, to give a variety of asymmetrical monosubstituted persistent triarylmethyl (TAM) radicals as the major products. The only by-products were symmetrical TAMs.
Библиографическая ссылка:
Tormyshev V.M.
, Rogozhnikova O.Y.
, Bowman M.K.
, Trukhin D.V.
, Troitskaya T.I.
, Vasiliev V.G.
, Shundrin L.A.
, Halpern H.J.
Preparation of Diversely Substituted Triarylmethyl Radicals by the Quenching of Tris(2,3,5,6-tetrathiaaryl)methyl Cations with C-, N-, P-, and S-Nucleophiles
European Journal of Organic Chemistry. 2014.
V.2014. N2. P.371-380. DOI: 10.1002/ejoc.201301161
WOS
Scopus
РИНЦ
OpenAlex
Preparation of Diversely Substituted Triarylmethyl Radicals by the Quenching of Tris(2,3,5,6-tetrathiaaryl)methyl Cations with C-, N-, P-, and S-Nucleophiles
Файлы:
Полный текст от издателя
Даты:
| Опубликована online: | 6 нояб. 2013 г. |
| Опубликована в печати: | 1 янв. 2014 г. |
Идентификаторы БД:
| Web of science: | WOS:000336266400012 |
| Scopus: | 2-s2.0-84891873467 |
| РИНЦ: | 21862759 |
| OpenAlex: | W1755783564 |