Unexpected Ring Opening During the Imination of Camphor‐Type Bicyclic Ketones | Sciact - CRIS-система Института катализа

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

Benzimidazoles; benzoxazoles; benzothiazoles; monoterpenoids; single-stage synthesis; norcamphor; (+)-camphor; (-)-fenchone

Авторы

Chernyshov Vladimir V. ^1,2 , Yarovaya Olga I. ^1,2 , Vatsadze Sergey Z. ⁴ , Borisevich Sophia S. ⁵ , Trukhan Sergey N. ^2,3 , Gatilov Yuri V. ^1,2 , Peshkov Roman Yu. ² , Eltsov Ilia V. ² , Martyanov Oleg N. ^2,3 , Salakhutdinov Nariman F. ^1,2

Организации

1	N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry SB RAS, 9 Acad. Lavrentiev Ave., 630090, Novosibirsk, Russian Federation
2	Novosibirsk State University, Pirogova St. 1, 630090, Novosibirsk, Russian Federation
3	Boreskov Institute of Catalysis SB RAS, 5 Acad. Lavrentiev Ave., 630090, Novosibirsk, Russian Federation
4	N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninski pr., 47, 119991 Moscow, Russian Federation
5	Laboratory of Chemical Physics, Ufa Institute of Chemistry, Ufa Federal Research Center, Russian Academy of Sciences, 71 Octyabrya pr., 450054, Ufa, Russian Federation

Информация о финансировании (1)

Российский фонд фундаментальных исследований

19-33-90080 (АААА-А19-119111490020-7)

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.

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 CAPlus OpenAlex

Поступила в редакцию:	21 окт. 2020 г.
Принята к публикации:	17 нояб. 2020 г.
Опубликована online:	19 нояб. 2020 г.
Опубликована в печати:	22 янв. 2021 г.

Web of science:	WOS:000602604300001
Scopus:	2-s2.0-85097617232
РИНЦ:	45079129
Chemical Abstracts:	2020:2623930
OpenAlex:	W3102924898

БД	Цитирований
Scopus	7
Web of science	7
РИНЦ	8
OpenAlex	9