Aryl iodides, bromides and vinyl-triflates are usually converted in high to excellent yields into the corresponding carboxylic acids through a parallel palladium-catalyzed hydroxycarbonylation using lithium formate and acetic anhydride as external condensed source of carbon monoxide.
Parallel palladium-catalyzed synthesis of carboxylic acids from aryl iodides, bromides, and vinyl triflates using acetic anhydride and formate anion as an external condensed source of carbon monoxide / Iazzetti, A.; Fabrizi, G.; Gazzilli, Y.; Goggiamani, A.; Marrone, F.; Shen, C.; Zoppoli, R.. - In: MOLECULES. - ISSN 1420-3049. - 30:15(2025), pp. 1-13. [10.3390/molecules30153298]
Parallel palladium-catalyzed synthesis of carboxylic acids from aryl iodides, bromides, and vinyl triflates using acetic anhydride and formate anion as an external condensed source of carbon monoxide
Fabrizi G.;Gazzilli Y.;Goggiamani A.
;Marrone F.;Shen C.;Zoppoli R.
2025
Abstract
Aryl iodides, bromides and vinyl-triflates are usually converted in high to excellent yields into the corresponding carboxylic acids through a parallel palladium-catalyzed hydroxycarbonylation using lithium formate and acetic anhydride as external condensed source of carbon monoxide.| File | Dimensione | Formato | |
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