Dual Acridine/Decatungstate Photocatalysis for the Decarboxylative Radical Addition of Carboxylic Acids to Azomethines Full article
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Organic Letters
ISSN: 1523-7060 , E-ISSN: 1523-7052 |
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| Output data | Year: 2024, Volume: 26, Number: 15, Pages: 3174-3178 Pages count : 5 DOI: 10.1021/acs.orglett.4c00778 | ||
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Abstract:
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.
Cite:
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 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 Scopus OpenAlex
Identifiers:
| Scopus: | 2-s2.0-85189975472 |
| OpenAlex: | W4394568107 |