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Generation of Trityl Radicals by Nucleophilic Quenching of Tris(2,3,5,6-tetrathiaaryl)methyl Cations and Practical and Convenient Large-Scale Synthesis of Persistent Tris(4-carboxy-2,3,5,6-tetrathiaaryl)methyl Radical Научная публикация

Журнал European Journal of Organic Chemistry
ISSN: 1434-193X , E-ISSN: 1099-0690
Вых. Данные Год: 2013, Том: 2013, Номер: 16, Страницы: 3347-3355 Страниц : DOI: 10.1002/ejoc.201300176
Ключевые слова Radicals; Carbocations; Quinones; Reaction mechanisms; Synthesis design
Авторы Rogozhnikova Olga Yu 1 , Vasiliev Vladimir G. 1 , Troitskaya Tatiana I. 1 , Trukhin Dmitry V. 1 , Mikhalina Tatiana V. 1 , Halpern Howard J. 2 , Tormyshev Victor M. 1,3
Организации
1 (Данные Web of science) Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia
2 (Данные Web of science) Univ Chicago, Dept Radiat & Cellular Oncol, Ctr EPR Imaging Vivo Physiol, Chicago, IL 60637 USA
3 (Данные Web of science) Novosibirsk State Univ, Dept Nat Sci, Novosibirsk 630090, Russia

Реферат: Tris(2,3,5,6-tetrathiaaryl)methyl cations, which were generated from the corresponding triarylmethanols in the presence of strong acids, underwent reaction with nucleophiles to give trityl radicals, as the product of a one-electron reduction of the carbocation. Depending on the nature of the nucleophile, the only byproducts were either diamagnetic quinone methides or asymmetrical monosubstituted trityl radicals. Herein, we report a protocol for the large-scale synthesis of the Finland trityl, which has the advantage of high overall yield and reproducibility.
Библиографическая ссылка: Rogozhnikova O.Y. , Vasiliev V.G. , Troitskaya T.I. , Trukhin D.V. , Mikhalina T.V. , Halpern H.J. , Tormyshev V.M.
Generation of Trityl Radicals by Nucleophilic Quenching of Tris(2,3,5,6-tetrathiaaryl)methyl Cations and Practical and Convenient Large-Scale Synthesis of Persistent Tris(4-carboxy-2,3,5,6-tetrathiaaryl)methyl Radical
European Journal of Organic Chemistry. 2013. V.2013. N16. P.3347-3355. DOI: 10.1002/ejoc.201300176 WOS Scopus РИНЦ OpenAlex
Файлы: Полный текст от издателя
Даты:
Опубликована online: 15 апр. 2013 г.
Опубликована в печати: 1 июн. 2013 г.
Идентификаторы БД:
Web of science: WOS:000320175200016
Scopus: 2-s2.0-84878178574
РИНЦ: 20429981
OpenAlex: W1807436685
Цитирование в БД:
БД Цитирований
Web of science 57
Scopus 55
РИНЦ 50
OpenAlex 64
Альметрики: