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Photoreactions of Semi-Stiff-Diarylethenes Based on the Cyclohexenol Motif Научная публикация

Журнал Organic Letters
ISSN: 1523-7060 , E-ISSN: 1523-7052
Вых. Данные Год: 2024, Том: 26, Номер: 37, Страницы: 7841-7846 Страниц : 6 DOI: 10.1021/acs.orglett.4c02659
Авторы Sergeeva Ekaterina S. 1,2 , Svistova Anastasia A. 1,2 , Ushakov Igor A. 1 , Vologzhanina Anna V. 3 , Pavlov Dmitry V. 1 , Lyssenko Konstantin A. 4 , Shirinian Valerii Z. 5 , Lvov Andrey G. 1,2
Организации
1 A. E. Favorsky Irkutsk Institute of Chemistry of the Siberian Branch of the Russian Academy of Sciences, 1 Favorsky Street, Irkutsk 664033, Russia
2 Irkutsk National Research Technical University, 83, Lermontov Street, Irkutsk 664074, Russia
3 A. N. Nesmeyanov Institute of Organoelement Compounds of the Russian Academy of Sciences, 28 Vavilova Street, Moscow 119991, Russia
4 Department of Chemistry, Lomonosov Moscow State University, Moscow 119992, Russia
5 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47, Leninsky prospekt, 119991 Moscow, Russia

Реферат: Nonsymmetric diarylethenes with an additional “stiff” cyclohexenol ring undergo various types of tandem transformations launched by light-induced 6π-photocyclization. Among these, there are two novel reactions (formal [1,3]-H migration and complete aromatization to an anthracene derivative) as well as photorearrangement and formal methane elimination. This diverse reactivity demonstrates the great potential of semi-stiff-diarylethenes in synthetic photochemistry.
Библиографическая ссылка: Sergeeva E.S. , Svistova A.A. , Ushakov I.A. , Vologzhanina A.V. , Pavlov D.V. , Lyssenko K.A. , Shirinian V.Z. , Lvov A.G.
Photoreactions of Semi-Stiff-Diarylethenes Based on the Cyclohexenol Motif
Organic Letters. 2024. V.26. N37. P.7841-7846. DOI: 10.1021/acs.orglett.4c02659 WOS Scopus OpenAlex
Идентификаторы БД:
Web of science: WOS:001308677000001
Scopus: 2-s2.0-85203239797
OpenAlex: W4402318984
Цитирование в БД:
БД Цитирований
OpenAlex 4
Scopus 3
Web of science 3
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