Dual Acridine/Decatungstate Photocatalysis for the Decarboxylative Radical Addition of Carboxylic Acids to Azomethines Научная публикация
| Журнал |
Organic Letters
ISSN: 1523-7060 , E-ISSN: 1523-7052 |
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| Вых. Данные | Год: 2024, Том: 26, Номер: 15, Страницы: 3174-3178 Страниц : 5 DOI: 10.1021/acs.orglett.4c00778 | ||
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Реферат:
A concept for the dual use of acridine and tetrabutylammonium decatungstate photocatalysts in the reactions of carboxylic acids is proposed. Imines generated in situ from aldehydes and p-methoxyaniline, as well as other azomethines, were used as radical acceptors. The role of the decatungstate is believed to facilitate the turnover of the acridine photocatalyst by means of hydrogen atom transfer.
Библиографическая ссылка:
Rubanov Z.M.
, Levin V.V.
, Dilman A.D.
Dual Acridine/Decatungstate Photocatalysis for the Decarboxylative Radical Addition of Carboxylic Acids to Azomethines
Organic Letters. 2024. V.26. N15. P.3174-3178. DOI: 10.1021/acs.orglett.4c00778 WOS Scopus OpenAlex
Dual Acridine/Decatungstate Photocatalysis for the Decarboxylative Radical Addition of Carboxylic Acids to Azomethines
Organic Letters. 2024. V.26. N15. P.3174-3178. DOI: 10.1021/acs.orglett.4c00778 WOS Scopus OpenAlex
Идентификаторы БД:
| Web of science: | WOS:001200653300001 |
| Scopus: | 2-s2.0-85189975472 |
| OpenAlex: | W4394568107 |