Photoreactions of Semi-Stiff-Diarylethenes Based on the Cyclohexenol Motif Научная публикация
| Журнал |
Organic Letters
ISSN: 1523-7060 , E-ISSN: 1523-7052 |
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| Вых. Данные | Год: 2024, Том: 26, Номер: 37, Страницы: 7841-7846 Страниц : 6 DOI: 10.1021/acs.orglett.4c02659 | ||||||||||
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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
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 |