Unexpected Ring Opening During the Imination of Camphor-Type Bicyclic Ketones Научная публикация
Журнал |
European Journal of Organic Chemistry
ISSN: 1434-193X , E-ISSN: 1099-0690 |
||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
Вых. Данные | Год: 2021, Том: 2021, Номер: 3, Страницы: 452-463 Страниц : 12 DOI: 10.1002/ejoc.202001397 | ||||||||||
Ключевые слова | (−)-Fenchone; Benzimidazoles; Camphor; Monoterpenoids; Single-stage synthesis | ||||||||||
Авторы |
|
||||||||||
Организации |
|
Реферат:
A new ring opening reaction was found while attempting to isolate the imines from ortho-heteroatom substituted anilines and camphor-like bicyclic ketones. The benzoazoles containing a cyclopentanemethyl group at position 2 of the heterocycle were isolated instead of the expected imines. The detailed study of the transformation, including EPR experiments, revealed the most probable radical mechanism. The proposed reaction pathways were confirmed by quantum chemical calculations. The dichotomy of 1–2 and 2–3 bonds cleavage is discussed together with the evaluation of the stereochemical outcome of the reactions. The benzoazoles obtained via the new reaction are of particular interest for the medicinal chemistry. © 2020 Wiley-VCH GmbH
Библиографическая ссылка:
Chernyshov V.V.
, Yarovaya O.I.
, Vatsadze S.Z.
, Borisevich S.S.
, Trukhan S.N.
, Gatilov Y.V.
, Peshkov R.Y.
, Eltsov I.V.
, Martyanov O.N.
, Salakhutdinov N.F.
Unexpected Ring Opening During the Imination of Camphor-Type Bicyclic Ketones
European Journal of Organic Chemistry. 2021. V.2021. N3. P.452-463. DOI: 10.1002/ejoc.202001397 WOS Scopus РИНЦ
Unexpected Ring Opening During the Imination of Camphor-Type Bicyclic Ketones
European Journal of Organic Chemistry. 2021. V.2021. N3. P.452-463. DOI: 10.1002/ejoc.202001397 WOS Scopus РИНЦ
Даты:
Опубликована online: | 27 дек. 2020 г. |
Опубликована в печати: | 22 янв. 2021 г. |
Идентификаторы:
Web of science | WOS:000602604300001 |
Scopus | 2-s2.0-85097617232 |
РИНЦ | 45079129 |
OpenAlex | W3102924898 |